Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17683430
SLC5A1
1.000 0.120 22 32091713 missense variant G/A snv 4.9E-02 4.5E-02 1
rs7330796
TBC1D4
13 75324027 intron variant T/C snv 0.76 1
rs17271305
VPS13C
15 62040781 intron variant A/G;T snv 1