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: rs769455
rs769455
2 0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 0.700 1.000 1 2014 2014