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: rs1057519073
rs1057519073
2 0.923 0.036 X 47142418 missense variant C/T snp 0.700 1 2016 2016