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: rs767983680
rs767983680
1 16 1204058 missense variant C/A;G snv 1.9E-05 0.700 0
dbSNP: rs775271588
rs775271588
1 16 1220830 missense variant A/G snv 6.4E-05 1.4E-05 0.700 0