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: rs146597836
rs146597836
1 1.000 0.200 22 17189987 missense variant C/T snv 1.8E-03 1.6E-03 0.700 0
dbSNP: rs750868279
rs750868279
1 1.000 0.200 22 17203576 missense variant G/A snv 5.2E-05 4.9E-05 0.700 0