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: rs11551462
rs11551462
2 0.925 0.120 2 47160802 missense variant A/G snv 0.010 1.000 1 2017 2017
dbSNP: rs398124647
rs398124647
6 0.807 0.120 2 47161851 missense variant T/A;C snv 0.010 1.000 1 2017 2017