Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80338758
MED12
0.790 0.400 X 71127367 missense variant C/A;T snv 9
rs765417606
MED12
0.882 0.400 X 71124263 missense variant A/G snv 2.8E-05 8.6E-05 3
rs80338759
MED12
0.925 0.280 X 71127931 missense variant A/G snv 2