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: rs768623239
rs768623239
14 0.724 0.286 1 109689278 missense variant A/G snp 1.5E-05 0.010 1.000 1 2002 2002
dbSNP: rs2066853
rs2066853
AHR
18 0.685 0.464 7 17339486 missense variant G/A snp 0.15 0.22 0.010 1.000 1 2003 2003
dbSNP: rs4986826
rs4986826
AHR
7 0.821 0.179 7 17339533 missense variant G/A snp 7.8E-03 2.0E-02 0.010 1.000 1 2003 2003
dbSNP: rs121909218
rs121909218
12 0.734 0.286 10 87933145 missense variant G/A snp 0.010 1.000 1 2004 2004
dbSNP: rs2074647
rs2074647
3 0.923 0.107 14 72562470 missense variant G/A snp 9.0E-02 9.4E-02 0.010 1.000 1 2004 2004
dbSNP: rs535058571
rs535058571
3 0.923 0.107 4 74446545 missense variant G/A snp 0.010 1.000 1 2004 2004
dbSNP: rs753945960
rs753945960
3 0.923 0.107 4 74446542 G/A snp 1.6E-05 0.010 1.000 1 2004 2004
dbSNP: rs786204929
rs786204929
8 0.821 0.143 10 87933144 missense variant G/A snp 0.010 1.000 1 2004 2004
dbSNP: rs758272654
rs758272654
28 0.667 0.536 20 58909201 synonymous variant T/C snp 4.0E-06 0.020 1.000 2 2005 2005
dbSNP: rs1801282
rs1801282
77 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 0.010 1.000 1 2005 2005
dbSNP: rs1805192
rs1805192
75 0.545 0.679 3 12379739 missense variant C/G snp 0.010 1.000 1 2005 2005
dbSNP: rs386675647
rs386675647
7 0.801 0.179 4 69098619 missense variant AT/TC multinucleotide-polymorphism 0.010 1.000 1 2005 2005
dbSNP: rs7439366
rs7439366
11 0.784 0.286 4 69098620 missense variant T/C snp 0.56 0.56 0.010 1.000 1 2005 2005
dbSNP: rs28931615
rs28931615
13 0.756 0.214 4 1804426 missense variant C/A,T snp 3.2E-05 0.010 1.000 1 2006 2006
dbSNP: rs1109324
rs1109324
5 0.846 0.143 6 43762018 intergenic variant G/T snp 0.15 0.010 1.000 1 2007 2007
dbSNP: rs1130409
rs1130409
45 0.590 0.500 14 20456995 missense variant T/A,C,G snp 4.0E-06; 4.0E-06; 0.42 0.44 0.010 1.000 1 2007 2007
dbSNP: rs1136410
rs1136410
35 0.622 0.357 1 226367601 missense variant A/G snp 0.21 0.16 0.010 1.000 1 2007 2007
dbSNP: rs121913483
rs121913483
13 0.734 0.250 4 1801841 missense variant C/A,G,T snp 4.2E-06; 1.3E-05 3.2E-05 0.010 1.000 1 2007 2007
dbSNP: rs125701
rs125701
5 0.846 0.107 3 9748794 intergenic variant G/A snp 0.14 0.010 1.000 1 2007 2007
dbSNP: rs1547651
rs1547651
3 0.923 0.107 6 43762907 intergenic variant A/T snp 0.15 0.010 1.000 1 2007 2007
dbSNP: rs3024994
rs3024994
4 0.878 0.107 6 43775770 non coding transcript exon variant C/T snp 4.6E-02 0.010 1.000 1 2007 2007
dbSNP: rs3136820
rs3136820
7 0.801 0.179 14 20456995 missense variant snp 0.010 1.000 1 2007 2007
dbSNP: rs351855
rs351855
35 0.642 0.357 5 177093242 missense variant G/A snp 0.33 0.27 0.010 1.000 1 2007 2007
dbSNP: rs11249206
rs11249206
5 0.846 0.143 1 24951491 intron variant C/T snp 0.49 0.010 1.000 1 2008 2008
dbSNP: rs11466445
rs11466445
6 0.846 0.143 9 99105274 inframe deletion CGGCGGCGGC/C in-del 0.010 < 0.001 1 2008 2008