Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv 4
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 4
rs10283100
ENPP2
8 119583783 missense variant A/G;T snv 0.96 3
rs11545169
PSMD2
3 184302754 missense variant G/T snv 0.13 0.11 3
rs13322435 3 157077679 upstream gene variant A/G snv 0.46 3
rs147110934
ZNF628
19 55482069 missense variant G/T snv 1.4E-02 1.5E-02 3
rs1818782
DAB2 ; C9
5 39424526 intron variant A/C snv 0.56 3
rs2229742
NRIP1
21 14966851 missense variant G/C snv 7.9E-02 7.1E-02 3
rs2928148
INO80
15 41109352 intron variant G/A snv 0.44 3
rs34776209 7 23473474 upstream gene variant C/T snv 0.18 3
rs6533183
TET2-AS1 ; TET2
4 105212027 intron variant C/T snv 0.61 3
rs7076938
LOC105378493
10 114029616 intergenic variant C/T snv 0.69 3
rs72656010
PLAG1 ; CHCHD7
8 56209656 intron variant T/C snv 0.10 3
rs798489
GNA12 ; AMZ1
7 2762169 splice donor variant C/T snv 0.20 3
rs11867479
KCNJ16
17 70094066 intron variant C/A;T snv 2
rs11893688
ADAM17
2 9555153 intron variant C/T snv 0.64 2
rs12153596
EBF1
5 158983170 non coding transcript exon variant C/T snv 0.30 2
rs12446550 16 28532060 downstream gene variant G/A snv 0.36 2
rs12461110
NLRP11
19 55809297 missense variant G/A snv 0.32 0.26 2
rs12656216
SKP2
5 36160566 intron variant G/A snv 0.64 2
rs12909648
AKAP13
15 85681339 intron variant G/A snv 0.40 2