Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 7
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs7655625 1.000 0.040 4 144564763 intron variant T/C;G snv 7
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs1530440
CABCOCO1
1.000 0.040 10 61764833 intron variant C/T snv 0.15 6
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs381815
PLEKHA7
1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 6
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 6
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs1173766 5 32804422 intergenic variant T/C snv 0.57 5
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv 5
rs12940887
ZNF652
17 49325445 intron variant C/T snv 0.28 5
rs12946454
ACBD4 ; PLCD3
0.925 0.040 17 45130754 intron variant A/T snv 0.21 5
rs13082711 3 27496418 intergenic variant T/C snv 0.16 5
rs13209747 6 126794309 intron variant C/G;T snv 0.36 5
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5
rs16849225 2 164050310 intron variant C/T snv 0.19 5
rs1813353
CACNB2
10 18418519 intron variant T/C snv 0.29 5
rs2004776
AGT
1 230712956 intron variant C/G;T snv 5
rs2954033 8 125481504 intron variant A/G snv 0.76 5
rs3824755
CYP17A1
0.925 0.120 10 102836092 intron variant G/A;C;T snv 5