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: rs104893648
rs104893648
4 0.882 0.320 2 15945883 missense variant G/A;T snv 0.700 0
dbSNP: rs779000620
rs779000620
1 1.000 0.080 2 15942288 missense variant C/G snv 4.2E-06 7.0E-06 0.010 1.000 1 2006 2006