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: rs1357012145
rs1357012145
1 1.000 0.080 10 88678487 missense variant A/G snv 0.010 1.000 1 2000 2000
dbSNP: rs775189464
rs775189464
1 1.000 0.080 10 88678446 missense variant C/G;T snv 4.0E-06; 5.6E-05 0.010 1.000 1 1999 1999