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: rs1057518873
rs1057518873
1 2 32144990 missense variant C/G;T snv 0.700 0
dbSNP: rs121908511
rs121908511
2 1.000 0.080 2 32141905 missense variant C/T snv 0.700 0