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: rs757574299
rs757574299
2 1.000 0.080 1 65570511 missense variant C/G snv 1.6E-05 1.4E-05 0.010 1.000 1 2005 2005