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: rs187152753
rs187152753
1 1.000 0.080 18 60371593 missense variant C/T snv 5.6E-05 1.3E-04 0.810 1.000 1 2007 2007