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: rs4820599
rs4820599
6 0.925 0.160 22 24594246 intron variant A/G snv 0.43 0.700 1.000 2 2008 2011
dbSNP: rs1169313
rs1169313
6 12 121004867 intron variant T/A;C snv 0.700 1.000 1 2008 2008
dbSNP: rs4742971
rs4742971
1 9 105892815 intergenic variant G/C;T snv 0.700 1.000 1 2008 2008
dbSNP: rs5751901
rs5751901
1 22 24596299 intron variant T/C snv 0.39 0.700 1.000 1 2008 2008
dbSNP: rs5751902
rs5751902
2 1.000 0.080 22 24600663 intron variant C/T snv 0.29 0.700 1.000 1 2010 2010
dbSNP: rs671
rs671
116 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.700 1.000 1 2010 2010
dbSNP: rs1497406
rs1497406
1 1 16178825 intergenic variant A/G snv 0.47 0.800 1.000 3 2011 2019
dbSNP: rs1260326
rs1260326
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.800 1.000 2 2011 2018
dbSNP: rs339969
rs339969
2 15 60591082 intron variant C/A snv 0.68 0.800 1.000 2 2011 2018
dbSNP: rs4074793
rs4074793
1 5 52897294 intron variant A/G snv 6.6E-02 0.800 1.000 2 2011 2018
dbSNP: rs4581712
rs4581712
1 16 80463704 intron variant C/A snv 0.22 0.800 1.000 2 2011 2018
dbSNP: rs4835265
rs4835265
6 4 145900258 intron variant C/A snv 0.15 0.700 1.000 2 2011 2018
dbSNP: rs944002
rs944002
3 14 103106478 intron variant A/G snv 0.25 0.800 1.000 2 2011 2012
dbSNP: rs10513686
rs10513686
1 3 171007753 intron variant G/A snv 0.21 0.800 1.000 1 2011 2011
dbSNP: rs1076540
rs1076540
1 22 17957192 intron variant C/T snv 0.21 0.800 1.000 1 2011 2011
dbSNP: rs10908458
rs10908458
1 1 155154472 intergenic variant T/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs11066453
rs11066453
4 1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs1126617
rs1126617
1 6 24489424 missense variant C/T snv 0.29 0.31 0.700 1.000 1 2011 2011
dbSNP: rs12145922
rs12145922
2 1 88680551 intron variant C/A snv 0.57 0.800 1.000 1 2011 2011
dbSNP: rs12229654
rs12229654
20 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs12539316
rs12539316
6 0.925 0.120 7 73563568 downstream gene variant A/G snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs12968116
rs12968116
2 18 57655270 missense variant C/T snv 8.2E-02 8.0E-02 0.800 1.000 1 2011 2011
dbSNP: rs13030978
rs13030978
1 2 191252512 intron variant C/T snv 0.24 0.800 1.000 1 2011 2011
dbSNP: rs1335645
rs1335645
1 1 111141654 intron variant A/G;T snv 0.15 0.800 1.000 1 2011 2011
dbSNP: rs17145750
rs17145750
9 0.925 0.120 7 73612048 intron variant C/A;T snv 0.800 1.000 1 2011 2011