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: rs11643718
rs11643718
10 0.807 0.240 16 56899607 missense variant G/A snv 0.11 8.4E-02 0.030 0.667 3 2008 2012
dbSNP: rs12708965
rs12708965
1 1.000 0.040 16 56902407 missense variant C/T snv 3.1E-02 3.5E-02 0.010 1.000 1 2007 2007
dbSNP: rs13306673
rs13306673
3 1.000 0.040 16 56867019 intron variant C/T snv 0.10 0.13 0.010 1.000 1 2011 2011
dbSNP: rs1529927
rs1529927
1 1.000 0.040 16 56870675 missense variant C/G snv 1.6E-05; 0.98 0.98 0.010 1.000 1 2004 2004
dbSNP: rs7204044
rs7204044
1 1.000 0.040 16 56908797 intron variant A/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs772187470
rs772187470
1 1.000 0.040 16 56870221 missense variant C/T snv 1.6E-05 2.8E-05 0.010 1.000 1 2004 2004