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: rs1131692266
rs1131692266
1 1.000 10 104225491 missense variant G/T snv 0.800 0
dbSNP: rs147356105
rs147356105
1 1.000 10 104203727 missense variant A/G snv 8.8E-05 1.9E-04 0.800 0
dbSNP: rs376788209
rs376788209
1 1.000 10 104230656 missense variant G/A snv 1.2E-05 7.0E-06 0.800 0