Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs139418552
MAP3K3
17 63628323 intron variant G/A snv 4.5E-03 1
rs67817520
MAP3K3
17 63631768 intron variant C/T snv 9.3E-02 1
rs7209435
MAP3K3
17 63635604 intron variant T/A;C;G snv 1
rs3785574
MAP3K3 ; LOC101927898 ; STRADA
17 63685825 intron variant T/C snv 0.26 1
rs11658329
STRADA ; LOC101927898 ; MAP3K3
17 63685671 intron variant G/C snv 0.39 1