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: rs80356461
rs80356461
1 1.000 0.040 19 45768373 missense variant C/T snv 1.1E-04 2.0E-04 0.800 1.000 1 2007 2007
dbSNP: rs80356462
rs80356462
1 1.000 0.040 19 45767073 missense variant C/T snv 5.5E-05 9.1E-05 0.800 1.000 1 2007 2007
dbSNP: rs80356463
rs80356463
1 1.000 0.040 19 45766866 missense variant C/T snv 1.4E-05 0.800 1.000 1 2007 2007
dbSNP: rs80356464
rs80356464
1 1.000 0.040 19 45766066 missense variant G/A;T snv 2.5E-04; 4.1E-06 0.700 1.000 1 2007 2007