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 0.020 1.000 2 2011 2011
dbSNP: rs113994095
rs113994095
31 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 0.010 1.000 1 2011 2011
dbSNP: rs2307441
rs2307441
6 0.882 0.080 15 89318595 missense variant T/C snv 2.9E-02 2.7E-02 0.010 < 0.001 1 2018 2018
dbSNP: rs3087374
rs3087374
3 0.882 0.080 15 89316763 missense variant C/A snv 6.1E-02 6.2E-02 0.010 < 0.001 1 2018 2018