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: rs2306283
rs2306283
4 0.923 0.036 12 21176804 missense variant A/G,T snp 0.47 0.53 0.020 1.000 2 2010 2013
dbSNP: rs4149056
rs4149056
21 0.734 0.250 12 21178615 missense variant T/C snp 0.13 0.14 0.020 1.000 2 2010 2013
dbSNP: rs10748835
rs10748835
1 1.000 0.036 10 102900499 intron variant G/A snp 0.42 0.010 1.000 1 2012 2012
dbSNP: rs11066280
rs11066280
22 0.769 0.214 12 112379979 intron variant T/A snp 1.5E-02 0.010 1.000 1 2014 2014
dbSNP: rs1137101
rs1137101
41 0.605 0.679 1 65592830 missense variant A/G snp 0.51 0.53 0.010 1.000 1 2017 2017
dbSNP: rs11542041
rs11542041
19 0.707 0.357 19 44908690 missense variant C/T snp 6.4E-05 0.010 1.000 1 1988 1988
dbSNP: rs11575937
rs11575937
17 0.715 0.321 1 156136985 missense variant G/A,T snp 0.010 1.000 1 2013 2013
dbSNP: rs12229654
rs12229654
14 0.801 0.214 12 110976657 intergenic variant T/G snp 1.1E-02 0.010 1.000 1 2014 2014
dbSNP: rs1256046734
rs1256046734
2 0.923 0.071 1 65621409 A/G snp 0.010 1.000 1 2017 2017
dbSNP: rs150599989
rs150599989
2 0.923 0.071 19 47341767 missense variant G/A,C,T snp 4.0E-06; 9.6E-05 3.2E-05 0.010 1.000 1 2006 2006
dbSNP: rs17249754
rs17249754
13 0.878 0.107 12 89666809 intron variant G/A snp 0.15 0.010 1.000 1 2014 2014
dbSNP: rs174537
rs174537
8 0.801 0.179 11 61785208 non coding transcript exon variant G/T snp 0.30 0.010 1.000 1 2011 2011
dbSNP: rs1799883
rs1799883
26 0.679 0.250 4 119320747 missense variant T/A,C,G snp 0.73 0.74 0.010 < 0.001 1 2001 2001
dbSNP: rs1799945
rs1799945
152 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 0.010 1.000 1 1999 1999
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 2001 2001
dbSNP: rs1800562
rs1800562
175 0.463 0.714 6 26092913 missense variant G/A snp 3.3E-02 3.8E-02 0.010 1.000 1 1999 1999
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 2001 2001
dbSNP: rs1805192
rs1805192
75 0.545 0.679 3 12379739 missense variant C/G snp 0.010 1.000 1 2001 2001
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 2016 2016
dbSNP: rs2222823
rs2222823
4 0.923 0.071 3 123885940 intergenic variant T/A snp 0.14 0.010 1.000 1 2013 2013
dbSNP: rs2230806
rs2230806
18 0.715 0.214 9 104858586 missense variant C/T snp 0.32 0.37 0.010 1.000 1 2004 2004
dbSNP: rs2811712
rs2811712
4 0.923 0.071 9 21998036 intron variant G/A snp 0.85 0.010 1.000 1 2013 2013
dbSNP: rs387906568
rs387906568
9 0.769 0.107 19 44909020 missense variant C/G,T snp 7.3E-06; 7.3E-06 0.010 1.000 1 1997 1997
dbSNP: rs4994
rs4994
44 0.605 0.536 8 37966280 missense variant A/G snp 0.11 9.0E-02 0.010 < 0.001 1 2001 2001
dbSNP: rs764608096
rs764608096
1 1.000 0.036 7 99666966 missense variant C/T snp 2.8E-05 0.010 1.000 1 2013 2013