Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519087
MFSD2A
0.925 0.120 1 39967632 missense variant C/T snv 7.0E-06 4
rs199634446
STIL
1.000 0.120 1 47251165 missense variant G/A;C snv 4.4E-05; 4.0E-06 1