Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs4665965
MPV17
0.925 0.120 2 27313513 intron variant T/A;C snv 4
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs17762454
RREB1
0.925 0.120 6 7212967 non coding transcript exon variant C/T snv 0.25 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs13404446
TRIM54
0.925 0.120 2 27296386 intron variant G/A snv 0.42 4
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 3
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 3
rs4502156 1.000 0.080 15 62090956 intergenic variant T/C snv 0.55 3
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 3
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 3
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 3
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 3
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs1371614
DPYSL5
2 26930006 intron variant C/T snv 0.29 3
rs1783598
FCHSD2
1.000 0.080 11 73140418 intron variant C/G;T snv 3
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 3
rs2908289
GCK ; LOC105375257
1.000 0.080 7 44184343 intron variant G/A snv 0.20 3
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs4245555
GRB10
1.000 0.120 7 50593712 intron variant T/C snv 0.32 3
rs7651090
IGF2BP2
0.925 0.080 3 185795604 intron variant A/G snv 0.39 3
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 3
rs2305929
RBKS ; MRPL33 ; BABAM2-AS1 ; BABAM2
1.000 0.040 2 27891044 intron variant A/G snv 0.14 3