Source: ALL
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: rs12422149
rs12422149
SLCO2B1
7 0.827 0.120 11 75172532 missense variant G/A;T snv 0.18 0.010 1.000 1 2019 2019
dbSNP: rs77559646
rs77559646
ANO7
1 1.000 2 241195850 missense variant G/A snv 1.4E-02 1.4E-02 0.010 1.000 1 2019 2019