Gene: MED12 ×
Source: INFERRED ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs80338759
rs80338759
MED12
2 0.925 0.280 X 71127931 missense variant A/G snv 0.810 1.000 0 2007 2013
dbSNP: rs765417606
rs765417606
MED12
3 0.882 0.400 X 71124263 missense variant A/G snv 2.8E-05 8.6E-05 0.700 0
dbSNP: rs80338758
rs80338758
MED12
9 0.790 0.400 X 71127367 missense variant C/A;T snv 0.700 0