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: rs387906559
rs387906559
1 1.000 0.107 3 129172601 intron variant GCAGG/G. microsatellite 0.700 4 2001 2009
dbSNP: rs16995309
rs16995309
2 0.923 0.179 20 50581336 missense variant C/T snp 4.8E-03 4.0E-03 0.010 < 0.001 1 2005 2005
dbSNP: rs1800206
rs1800206
17 0.707 0.286 22 46218377 missense variant C/G snp 4.3E-02 4.0E-02 0.010 1.000 1 2004 2004
dbSNP: rs225014
rs225014
13 0.734 0.321 14 80203237 missense variant T/C snp 0.41 0.37 0.010 1.000 1 2010 2010
dbSNP: rs4986790
rs4986790
146 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 0.010 1.000 1 2011 2011
dbSNP: rs4986791
rs4986791
108 0.501 0.714 9 117713324 missense variant C/T snp 5.7E-02 5.1E-02 0.010 1.000 1 2011 2011
dbSNP: rs4994
rs4994
44 0.605 0.536 8 37966280 missense variant A/G snp 0.11 9.0E-02 0.010 1.000 1 2012 2012
dbSNP: rs696217
rs696217
24 0.685 0.536 3 10289773 missense variant G/T snp 8.8E-02 7.2E-02 0.010 1.000 1 2009 2009
dbSNP: rs750359414
rs750359414
3 0.923 0.179 19 7669884 missense variant C/G,T snp 4.0E-06; 4.0E-06 0.010 < 0.001 1 2005 2005
dbSNP: rs781057451
rs781057451
1 1.000 0.107 17 63972630 missense variant G/A snp 4.2E-06 0.010 1.000 1 2015 2015