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: rs775445970
rs775445970
1 1.000 0.080 15 89321783 missense variant T/C snv 4.0E-06 0.700 1.000 3 2008 2009