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: rs369925690
rs369925690
2 0.925 0.120 6 52071009 missense variant T/C;G snv 1.0E-04 0.700 1.000 4 2002 2010
dbSNP: rs745770404
rs745770404
2 0.925 0.120 6 52050157 missense variant C/T snv 1.6E-05 1.4E-05 0.700 1.000 4 2002 2010