Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs537841689 12 90550058 intergenic variant C/T snv 3.6E-04 1
rs765885335 6 104245432 intergenic variant A/G snv 3.6E-04 1
rs9810195 3 193028537 regulatory region variant A/G snv 0.16 1
rs541558502
FAM110B
8 58095231 intron variant G/A snv 1.0E-03 1
rs114864815
HCP5
6 31461210 intron variant C/T snv 1
rs75640364
HCP5
6 31465789 non coding transcript exon variant G/C snv 6.1E-02 1
rs17199328
HLA-B
6 31354618 non coding transcript exon variant A/C;G;T snv 4.0E-06; 9.8E-02 1
rs142765674
LINC02785
1 108070308 intron variant A/G snv 4.7E-03 1
rs147482218
LRRC32
11 76667642 intron variant T/G snv 7.9E-03 1
rs144721899
TMC7
16 18993889 intron variant A/G snv 3.4E-03 1