Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 14
rs6996224
STAU2
1.000 8 73568350 intron variant T/C snv 0.19 1