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: rs1057521065
rs1057521065
1 1.000 0.040 17 63968310 missense variant A/G snv 0.010 1.000 1 2010 2010
dbSNP: rs80338958
rs80338958
9 0.790 0.200 17 63945614 missense variant C/A;T snv 1.6E-05; 5.6E-05 0.010 1.000 1 2018 2018