Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 3
rs1011754
UBE2E2
1.000 0.080 3 23499566 intron variant A/G snv 4.2E-02 2.8E-02 1
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 1
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs10189773
ARHGAP15
1.000 0.080 2 143138931 intron variant A/G snv 0.20 1
rs10190052 1.000 0.080 2 646674 intergenic variant T/C snv 0.82 1
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs10203174
THADA
1.000 0.080 2 43462891 intron variant C/T snv 0.17 1
rs1020731
RBMS1
1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 4
rs10228456 1.000 0.080 7 15024301 intergenic variant C/T snv 0.54 2
rs10229583 1.000 0.080 7 127606849 downstream gene variant G/A snv 0.23 1
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs10258074 1.000 0.080 7 15024591 intergenic variant A/T snv 0.54 1
rs10258162
LOC105375490
1.000 0.080 7 127518569 intergenic variant C/T snv 0.42 1
rs10261386
CPED1
1.000 0.080 7 121071801 intron variant C/T snv 0.38 1
rs1027700
ATF6
1.000 0.080 1 161787246 intron variant A/T snv 0.21 1
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs1040558
CDKAL1
1.000 0.080 6 20713475 intron variant A/G snv 0.19 1
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 2
rs10440833
CDKAL1
1.000 0.080 6 20687890 intron variant T/A;G snv 0.26 1
rs1045493
ZSWIM3
1.000 0.080 20 45877779 synonymous variant G/A snv 0.56 0.52 1
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs10487796 1.000 0.080 7 15023805 intergenic variant T/A snv 0.40 1