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: rs113994097
rs113994097
22 0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 0.010 1.000 1 2010 2010
dbSNP: rs113994098
rs113994098
12 0.742 0.320 15 89321792 missense variant C/T snv 1.5E-04 2.7E-04 0.010 1.000 1 2010 2010
dbSNP: rs267606959
rs267606959
19 0.732 0.200 15 89318986 missense variant G/A snv 2.0E-05 0.010 1.000 1 2010 2010
dbSNP: rs3087374
rs3087374
3 0.882 0.080 15 89316763 missense variant C/A snv 6.1E-02 6.2E-02 0.010 1.000 1 2014 2014