Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2074404
LRRC37A2 ; WNT3
0.925 0.120 17 46788073 intron variant T/G snv 0.27 2
rs2735421
NPM3 ; FGF8
10 101781259 upstream gene variant T/G snv 0.65 2
rs302719
RERE-AS1 ; RERE
1.000 0.040 1 8430260 intron variant T/G snv 0.33 2
rs67450615 2 156636780 intergenic variant T/G snv 0.15 2
rs6949851 7 32454195 downstream gene variant T/G snv 0.33 2
rs7602651
RAB11FIP5
1.000 0.040 2 73109679 intron variant T/G snv 0.34 2
rs7616632 3 137312395 intergenic variant T/G snv 0.41 2
rs80170948
SREK1IP1
5 64724489 missense variant T/G snv 3.0E-02 2.8E-02 2
rs10218712
FOXO6
1 41366625 intron variant T/G snv 0.34 1
rs10273635
LOC105375490
7 127518303 intergenic variant T/G snv 0.64 1
rs1050331
ZMIZ2
7 44768492 3 prime UTR variant T/G snv 0.50 1
rs10992853
PHF2
9 93674643 intron variant T/G snv 0.34 1
rs11130226
RBM6
3 49955758 intron variant T/G snv 0.48 1
rs114151376
ZFYVE9
1 52280829 intron variant T/G snv 5.4E-02 1
rs115028891
EIF5B
2 99346967 intron variant T/G snv 1.2E-02 1
rs11634187
IVD
15 40430582 intron variant T/G snv 0.12 1
rs11720236 3 127442846 intergenic variant T/G snv 0.13 1
rs12439619
EFL1
15 82254605 intron variant T/G snv 0.27 1
rs12736566
SLFNL1-AS1 ; SLFNL1
1 41018479 intron variant T/G snv 1.9E-02 1
rs12772375
GBF1
10 102322931 intron variant T/G snv 0.48 1
rs13253386
SGCZ
8 14144511 intron variant T/G snv 0.38 1
rs13411858
SMARCAL1
2 216441975 intron variant T/G snv 0.23 1
rs143283559
KCNG2
18 79807761 intron variant T/G snv 0.27 1
rs1514506 8 65262315 intergenic variant T/G snv 0.97 1
rs1550404
LOC105373602
2 126573377 intergenic variant T/G snv 5.1E-02 1