Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75686861
HHIP
0.790 0.080 4 144700176 intron variant G/A snv 6.3E-02 10
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs10737680
CFH
0.827 0.080 1 196710325 intron variant A/C snv 0.44 7
rs550057
ABO
0.925 0.080 9 133271182 intron variant T/A;C snv 7
rs2869966
LOC105377327 ; FAM13A
1.000 0.040 4 88947927 intron variant C/T snv 0.47 6
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs13116999
LOC105377462
4 144521212 intron variant G/A snv 0.65 4
rs1513272
JAZF1
7 28160478 intron variant C/T snv 0.40 4
rs2076295
DSP
0.882 0.080 6 7562999 intron variant T/G snv 0.46 4
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39 4
rs442177
AFF1
4 87109109 intron variant G/T snv 0.56 4
rs6780171
IGF2BP2
3 185785668 intron variant T/A snv 0.39 4
rs6918725
LOC105377992
6 126669246 intron variant T/G snv 0.50 4
rs7424771
RBMS1
2 160419867 intron variant G/A snv 0.44 4
rs7752448
ZSCAN31
6 28333322 intron variant A/G snv 0.15 4
rs8042849
HYKK
1.000 0.040 15 78525587 intron variant C/T snv 0.65 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs1008833
PIK3C2B
1 204457167 intron variant A/G snv 0.12 3
rs10998018
MYPN
10 68203197 intron variant G/A snv 0.41 3
rs11012732
MLLT10
0.882 0.080 10 21541175 intron variant A/G snv 0.31 3
rs1102077 6 139950220 intron variant A/C snv 0.21 3
rs11621587
RIN3
14 92631994 intron variant G/C;T snv 3
rs11722225
INTS12 ; GSTCD
4 105845273 intron variant T/C snv 5.5E-02 3
rs12513481
AP3B1
5 78155004 intron variant G/C snv 0.19 3
rs12825748
MSRB3
12 65399373 intron variant G/C snv 0.28 3