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: rs1800463
rs1800463
2 1.000 0.040 14 94614674 missense variant T/A;C snv 0.030 1.000 3 1993 2000