Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs10255839
EVX1
7 27249498 intron variant G/A snv 0.87 6
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs1495743 8 18415790 intergenic variant G/A;C snv 6
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs62434129
PLEKHG1
6 150687701 intron variant A/G;T snv 8.8E-02 6
rs9292468 5 32818967 intergenic variant T/A;C snv 6