Source: INFERRED ×
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: rs113488022
rs113488022
22 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 0.800 1.000 1 2011 2019
dbSNP: rs121913361
rs121913361
6 0.807 0.280 7 140753349 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs397507483
rs397507483
13 0.790 0.400 7 140753348 missense variant C/A;T snv 0.700 1.000 1 2016 2016