Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10900586
ATP2B4
1 203684957 intron variant G/A snv 0.83 2
rs10923398 1 117708553 regulatory region variant A/C snv 0.16 2
rs10926973
CEP170
1 243225068 intron variant A/T snv 0.39 2
rs10950673
SUN1
7 835002 intron variant A/G snv 0.17 2
rs10952780
EZH2
7 148857243 intron variant A/C snv 0.46 2
rs10971957 9 34151465 regulatory region variant C/T snv 0.51 2
rs10981250
SUSD1
9 112076741 intron variant G/T snv 0.11 2
rs10988207
CRAT
9 129104851 intron variant G/A;C;T snv 2
rs10991473 9 105024605 downstream gene variant G/A;C snv 2
rs11021221 11 95575690 intron variant T/A;G snv 4
rs11023895
SOX6
11 16264638 3 prime UTR variant G/A;C snv 2
rs11030967
RRM1
11 4107890 intron variant C/T snv 0.51 2
rs1105291
RCCD1
15 90959153 intron variant C/T snv 0.13 2
rs11065156
RNF10
12 120544273 intron variant A/G snv 1.4E-02 2
rs11065589
KDM2B
12 121483077 intron variant C/G;T snv 2
rs11082513 18 46167187 intergenic variant C/T snv 0.42 3
rs11097044
G3BP2
4 75643297 3 prime UTR variant A/C;T snv 2
rs11103379
LHX3
9 136205504 upstream gene variant A/C snv 0.48 2
rs11117363 16 88086625 intron variant A/C;G snv 2
rs11119784
LINC01693
1 211641622 intron variant C/A;T snv 2
rs11122449
GALNT2
1 230164735 intron variant C/G;T snv 0.56 2
rs11133613
SLC12A7
5 1074936 intron variant A/G snv 0.91 2
rs111527163 4 68732288 intergenic variant A/T snv 0.19 2
rs111660650
LOC101928277
6 134826438 regulatory region variant C/T snv 1.3E-02 2
rs111871296
ATP7B ; ALG11
13 52012616 intron variant G/A snv 4.2E-02 2