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: rs104894677
rs104894677
2 0.925 0.080 19 51347006 missense variant C/T snv 4.0E-06 7.0E-06 0.700 1.000 2 1994 2003
dbSNP: rs104894678
rs104894678
2 0.925 0.080 19 51350385 missense variant C/T snv 1.7E-05 2.1E-05 0.700 1.000 2 1994 2003