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: rs1554411234
rs1554411234
5 1.000 7 50463322 missense variant C/A snv 0.700 0
dbSNP: rs771317809
rs771317809
6 0.925 0.080 7 50470140 missense variant C/T snv 8.0E-06 0.700 0