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: rs532738858
rs532738858
1 1.000 0.080 4 105236763 missense variant C/T snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs376570662
rs376570662
1 1.000 0.080 4 105235321 missense variant C/T snv 1.2E-04 1.7E-04 0.700 0
dbSNP: rs114619974
rs114619974
1 1.000 0.080 4 105234376 missense variant G/A snv 5.2E-04 2.2E-03 0.700 0