Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs2075064
LHX2
9 124021568 intron variant C/T snv 0.35 1
rs6440003
ZBTB38
3 141375367 intron variant G/A snv 0.54 1
rs2222328
IQCJ-SCHIP1 ; SCHIP1
3 159541502 intron variant T/C snv 0.17 1
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 4
rs10913469
SEC16B ; CRYZL2P-SEC16B
1.000 0.080 1 177944384 intron variant T/C snv 0.22 5
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 3
rs12446632
LOC105371116
1.000 0.080 16 19924067 intergenic variant G/A snv 0.11 1
rs1440072
KCNE4
2 223072020 intron variant C/A;G;T snv 1
rs7654585 4 25941129 intergenic variant A/G snv 0.60 1
rs806794
H2AC7 ; H3C4 ; H2BC7
6 26200449 3 prime UTR variant A/G snv 0.36 2
rs7601155
BABAM2
2 28124815 intron variant C/T snv 6.8E-02 1
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 3
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 1
rs11847697
PRKD1
14 30045906 intron variant C/T snv 0.13 2
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 2
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 2
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs7132908
FAIM2
1.000 0.080 12 49869365 3 prime UTR variant G/A snv 0.31 1
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 3
rs7206790
FTO
0.925 0.160 16 53763996 intron variant C/G snv 0.49 2