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: rs121434601
rs121434601
3 0.925 0.080 3 46898097 missense variant C/T snv 1.7E-03 1.7E-03 0.720 1.000 2 2004 2008
dbSNP: rs137854532
rs137854532
4 0.882 0.160 20 58905443 missense variant C/T snv 0.010 1.000 1 2008 2008