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: rs1135401818
rs1135401818
1 1.000 1 7677682 missense variant C/T snv 0.700 1.000 1 2015 2015