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: rs10756819
rs10756819
1 1.000 0.120 9 16858086 intron variant G/A;C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs10810666
rs10810666
1 1.000 0.120 9 16911668 intergenic variant C/T snv 0.14 0.700 1.000 1 2009 2009
dbSNP: rs10962656
rs10962656
1 1.000 0.120 9 16877790 intergenic variant G/A snv 0.10 0.700 1.000 1 2009 2009
dbSNP: rs12379183
rs12379183
1 1.000 0.120 9 16865701 intron variant A/G snv 0.26 0.700 1.000 1 2009 2009
dbSNP: rs12379687
rs12379687
1 1.000 0.120 9 16854369 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs12451939
rs12451939
1 1.000 0.120 17 61970281 intron variant A/G snv 2.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs12937080
rs12937080
1 1.000 0.120 17 61852376 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12938171
rs12938171
1 1.000 0.120 17 61902994 intron variant G/A snv 9.0E-03 0.700 1.000 1 2011 2011
dbSNP: rs1339552
rs1339552
1 1.000 0.120 9 16848792 intron variant C/T snv 0.52 0.700 1.000 1 2009 2009
dbSNP: rs1416742
rs1416742
1 1.000 0.120 9 16856885 intron variant G/A snv 0.43 0.700 1.000 1 2009 2009
dbSNP: rs4445329
rs4445329
1 1.000 0.120 9 16911759 intergenic variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs4961501
rs4961501
1 1.000 0.120 9 16851680 intron variant T/A;C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs7861573
rs7861573
1 1.000 0.120 9 16862282 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs1199923024
rs1199923024
1 1.000 0.120 17 61683945 missense variant G/A snv 1.6E-05 7.0E-06 0.700 0
dbSNP: rs121913340
rs121913340
1 1.000 0.120 7 140753379 missense variant C/T snv 0.700 0
dbSNP: rs1800726
rs1800726
1 1.000 0.120 17 43070993 missense variant C/G;T snv 0.700 0
dbSNP: rs1800757
rs1800757
1 1.000 0.120 17 43051069 missense variant G/A snv 0.700 0
dbSNP: rs35394823
rs35394823
1 1.000 0.120 17 2040586 missense variant C/G snv 8.1E-02 6.8E-02 0.700 0
dbSNP: rs372000848
rs372000848
1 1.000 0.120 11 94470575 missense variant G/A snv 5.2E-05 7.7E-05 0.700 0
dbSNP: rs56070345
rs56070345
1 1.000 0.120 13 32356497 missense variant G/A;C;T snv 6.4E-05 0.700 0
dbSNP: rs778705666
rs778705666
1 1.000 0.120 17 2030174 missense variant C/T snv 0.700 0
dbSNP: rs80357462
rs80357462
1 1.000 0.120 17 43057083 missense variant G/A;C snv 0.700 0
dbSNP: rs80358479
rs80358479
1 1.000 0.120 13 32333367 missense variant C/T snv 2.1E-04 1.2E-04 0.700 0
dbSNP: rs80359176
rs80359176
1 1.000 0.120 13 32380076 missense variant C/T snv 3.6E-05 7.0E-06 0.700 0
dbSNP: rs137852691
rs137852691
2 0.925 0.120 11 132657203 missense variant G/A;C snv 8.0E-06 0.700 1.000 3 2008 2013