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: rs761564262
rs761564262
1 1.000 19 43546884 missense variant C/G snv 3.2E-05 0.700 1.000 1 2017 2017