Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10211296
CSRNP3
1.000 0.080 2 165633833 intron variant A/G snv 0.34 3
rs10483038
KCNJ6
1.000 0.080 21 37652469 intron variant T/C snv 0.26 3
rs11075992
FTO
1.000 0.080 16 53786154 intron variant T/C snv 0.41 3
rs111372083
KCNJ6
1.000 0.080 21 37638374 intron variant C/A;T snv 0.27 3
rs111576572
KCNJ6
1.000 0.080 21 37617262 3 prime UTR variant A/G snv 0.32 3
rs1154433
ADH1B
1.000 0.080 4 99332551 intron variant A/G;T snv 3
rs115460205
FSTL5
1.000 0.080 4 161890417 intron variant C/T snv 4.7E-02 3
rs12482570
LOC107985507 ; KCNJ6
1.000 0.080 21 37705475 intron variant A/G snv 0.30 3
rs12639833
ADH1C ; ADH1B
1.000 0.080 4 99346215 intron variant C/T snv 0.31 3
rs12898370
HMG20A
1.000 0.080 15 77516256 intergenic variant A/C;T snv 3
rs12898460
LINC02694
0.882 0.080 15 38694612 intron variant C/T snv 0.23 3
rs12912251
LINC02694
0.882 0.080 15 38694167 intron variant G/T snv 0.25 3
rs1316543
GRK5
1.000 0.080 10 119445148 intron variant G/A snv 0.15 3
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 3
rs1399590
KCNJ6
1.000 0.080 21 37681768 intron variant G/A snv 0.56 3
rs1399591
KCNJ6
1.000 0.080 21 37681654 intron variant C/T snv 0.50 3
rs1399592
KCNJ6
1.000 0.080 21 37681559 intron variant T/A;G snv 0.52 3
rs141424017 1.000 0.080 7 115311376 intergenic variant -/CAA ins 3
rs1437396 1.000 0.080 2 55278320 upstream gene variant C/G;T snv 3
rs1475839
KCNJ6
1.000 0.080 21 37649639 intron variant C/T snv 0.31 3
rs1515050
KCNJ6
1.000 0.080 21 37630840 intron variant T/C snv 0.75 3
rs1515056
LOC107985507 ; KCNJ6
1.000 0.080 21 37710283 intron variant C/G;T snv 0.28 3
rs1612735
ADH1B ; ADH1C
1.000 0.080 4 99336850 intron variant T/C snv 0.31 3
rs1614972
ADH1B ; ADH1C
0.925 0.160 4 99336998 intron variant C/T snv 0.38 3
rs1660895 1.000 0.080 2 129236759 intergenic variant A/T snv 0.52 3