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: rs1047781
rs1047781
11 0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 0.010 1.000 1 2016 2016
dbSNP: rs281377
rs281377
4 0.925 0.120 19 48703346 synonymous variant C/T snv 0.49 0.42 0.010 1.000 1 2016 2016