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: rs77103971
rs77103971
2 0.925 0.120 19 12810323 missense variant C/T snv 4.0E-06 2.8E-05 0.700 1.000 4 2007 2013