chrom	pos	variation	variant_type	snp_id	clinical_significance	validation_status	function_class	gene	frequency
chr6	1500074	G>A,C,T	snv	7769815		by-frequency;by-alfa;by-cluster	intron_variant;genic_upstream_transcript_variant;genic_downstream_transcript_variant	LOC102723944;LOC124901238	A:0.456433:2286:1000Genomes|G:0.488843:1884:ALSPAC|G:0.495982:2222:Estonian|G:0.475:19:GENOME_DK|A:0.433663:60686:GnomAD|G:0.492986:492:GoNL|G:0.37099:1087:KOREAN|G:0.381004:698:Korea1K|A:0.481667:289:NorthernSweden|A:0.342593:74:Qatari|G:0.285714:116:SGDP_PRJ|G:0.315789:12:Siberian|G:0.393375:6593:TOMMO|A:0.428089:113311:TOPMED|G:0.478695:1775:TWINSUK|G:0.336449:72:Vietnamese|T:0.:0:ALFA
chr6	1500038	G>A	snv	543909390		by-frequency;by-alfa;by-cluster	genic_downstream_transcript_variant;genic_upstream_transcript_variant;intron_variant	LOC102723944;LOC124901238	A:0.000781:4:1000Genomes|A:0.000706:99:GnomAD|G:0.5:1:SGDP_PRJ|A:0.00062:164:TOPMED|A:0.000285:4:ALFA
chr6	1500049	G>C	snv	561609009		by-frequency;by-cluster	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	C:0.0003:2:1000Genomes
chr6	1500020	T>C	snv	749293473		by-frequency;by-alfa;by-cluster	genic_downstream_transcript_variant;genic_upstream_transcript_variant;intron_variant	LOC102723944;LOC124901238	C:0.000007:1:GnomAD|C:0.000035:1:TOMMO|C:0.000015:4:TOPMED|C:0.:0:ALFA
chr6	1500040	C>T	snv	781213609		by-frequency;by-alfa;by-cluster	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	T:0.000259:1:ALSPAC|T:0.000021:3:GnomAD|T:0.000034:9:TOPMED|T:0.00027:1:TWINSUK|T:0.:0:ALFA
chr6	1500053	G>A	snv	907499033		by-frequency;by-alfa;by-cluster	genic_downstream_transcript_variant;genic_upstream_transcript_variant;intron_variant	LOC102723944;LOC124901238	A:0.000015:4:TOPMED|A:0.:0:ALFA
chr6	1500052	G>T	snv	916907879		by-frequency;by-alfa	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	T:0.000008:2:TOPMED|T:0.:0:ALFA
chr6	1500028	C>T	snv	930001740		by-frequency;by-alfa;by-cluster	genic_downstream_transcript_variant;genic_upstream_transcript_variant;intron_variant	LOC102723944;LOC124901238	T:0.000007:1:GnomAD|T:0.000008:2:TOPMED|T:0.000071:1:ALFA
chr6	1500073	C>T	snv	1044133166		by-frequency;by-alfa;by-cluster	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	T:0.000007:1:GnomAD|T:0.000011:3:TOPMED|T:0.:0:ALFA
chr6	1500062	A>T	snv	1172428049		by-frequency;by-alfa	intron_variant;genic_upstream_transcript_variant;genic_downstream_transcript_variant	LOC102723944;LOC124901238	T:0.000004:1:TOPMED|T:0.:0:ALFA
chr6	1500081	C>G	snv	1188316840		by-frequency;by-alfa	genic_upstream_transcript_variant;intron_variant;genic_downstream_transcript_variant	LOC102723944;LOC124901238	G:0.:0:ALFA
chr6	1500092	T>C	snv	1220019657		by-frequency;by-alfa;by-cluster	genic_downstream_transcript_variant;intron_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	C:0.000007:1:GnomAD|C:0.000004:1:TOPMED|C:0.:0:ALFA
chr6	1500063	A>C,G	snv	1245759039		by-frequency;by-alfa;by-cluster	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	G:0.000004:1:TOPMED|G:0.:0:ALFA
chr6	1500099	T>A	snv	1256360852		by-frequency;by-alfa	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	A:0.000008:2:TOPMED|A:0.:0:ALFA
chr6	1500079	G>A	snv	1355322853		by-frequency;by-alfa	genic_downstream_transcript_variant;genic_upstream_transcript_variant;intron_variant	LOC102723944;LOC124901238	A:0.:0:GnomAD|A:0.:0:ALFA
chr6	1500071	T>C	snv	1420602999		by-frequency;by-alfa;by-cluster	genic_upstream_transcript_variant;intron_variant;genic_downstream_transcript_variant	LOC102723944;LOC124901238	C:0.000007:1:GnomAD|C:0.000004:1:TOPMED|C:0.:0:ALFA
chr6	1500093	T>C	snv	1457422616		by-frequency;by-alfa	genic_upstream_transcript_variant;genic_downstream_transcript_variant;intron_variant	LOC102723944;LOC124901238	C:0.000004:1:TOPMED|C:0.:0:ALFA
chr6	1500001	G>A	snv	1760712897		by-frequency;by-alfa	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	A:0.000004:1:TOPMED|A:0.:0:ALFA
chr6	1500016	C>G	snv	1760712924		by-frequency;by-alfa	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	G:0.000004:1:TOPMED|G:0.:0:ALFA
chr6	1500029	A>G	snv	1760713013		by-frequency;by-alfa;by-cluster	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	G:0.000007:1:GnomAD|G:0.000004:1:TOPMED|G:0.:0:ALFA
chr6	1500037	G>A	snv	1760713045		by-frequency;by-alfa	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	A:0.000004:1:TOPMED|A:0.:0:ALFA
chr6	1500045	C>A	snv	1760713132		by-frequency;by-alfa;by-cluster	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	A:0.000007:1:GnomAD|A:0.000004:1:TOPMED|A:0.:0:ALFA
chr6	1500048	T>C	snv	1760713161		by-frequency;by-alfa	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	C:0.000004:1:TOPMED|C:0.:0:ALFA
chr6	1500055	G>T	snv	1760713285		by-frequency;by-alfa	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	T:0.:0:ALFA
chr6	1500067	C>T	snv	1760713364		by-frequency;by-alfa	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	T:0.:0:ALFA
chr6	1500070	A>G	snv	1760713390		by-frequency;by-alfa	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	G:0.000004:1:TOPMED|G:0.:0:ALFA
chr6	1500078	G>C	snv	1760713592		by-frequency;by-alfa	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	C:0.:0:ALFA
chr6	1500085	C>A	snv	1760713657		by-frequency;by-cluster	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	A:0.00004:1:TOMMO
chr6	1500100	G>T	snv	1760713774		by-frequency;by-alfa	intron_variant;genic_downstream_transcript_variant;genic_upstream_transcript_variant	LOC102723944;LOC124901238	T:0.000004:1:TOPMED|T:0.000094:1:ALFA
chr6	1500087	C>T	snv	2113473571		by-frequency	genic_upstream_transcript_variant;genic_downstream_transcript_variant;intron_variant	LOC102723944;LOC124901238	T:0.00007:2:TOMMO
chr6	1500074	G>A,C,T	snv	7769815		by-frequency;by-alfa;by-cluster	intron_variant;genic_upstream_transcript_variant;genic_downstream_transcript_variant	LOC102723944;LOC124901238	A:0.456433:2286:1000Genomes|G:0.488843:1884:ALSPAC|G:0.495982:2222:Estonian|G:0.475:19:GENOME_DK|A:0.433663:60686:GnomAD|G:0.492986:492:GoNL|G:0.37099:1087:KOREAN|G:0.381004:698:Korea1K|A:0.481667:289:NorthernSweden|A:0.342593:74:Qatari|G:0.285714:116:SGDP_PRJ|G:0.315789:12:Siberian|G:0.393375:6593:TOMMO|A:0.428089:113311:TOPMED|G:0.478695:1775:TWINSUK|G:0.336449:72:Vietnamese|T:0.:0:ALFA
