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: rs28934574
rs28934574
4 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 1997 1997
dbSNP: rs28934576
rs28934576
47 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 0.010 1.000 1 1997 1997