Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 25
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 6
rs2294214
CASC15
0.882 0.040 6 22056694 splice region variant A/C;T snv 6
rs2812378
CCL21
0.790 0.200 9 34710263 intron variant G/A;C snv 6
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs2066845
NOD2
0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 5
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 5
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 4
rs9844972 1.000 0.080 3 150379848 regulatory region variant G/A;C snv 4
rs1030431 8 58399138 intergenic variant A/G;T snv 3