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: rs1333037
rs1333037
3 0.923 0.036 9 22040766 intron variant C/T snp 0.70 0.700 1 2016 2016
dbSNP: rs2041895
rs2041895
1 1.000 0.036 12 106956310 intron variant C/A,G snp 3.2E-05; 0.56 0.700 1 2016 2016
dbSNP: rs284491
rs284491
2 0.923 0.036 8 104946405 intron variant C/T snp 0.46 0.700 1 2016 2016
dbSNP: rs28939688
rs28939688
6 0.801 0.107 10 13109270 missense variant G/A snp 0.040 1.000 4 2003 2014
dbSNP: rs11258194
rs11258194
7 0.801 0.143 10 13110400 missense variant T/A snp 4.4E-02 6.1E-02 0.030 1.000 3 2003 2006
dbSNP: rs10120688
rs10120688
5 0.846 0.107 9 22056500 intron variant G/A snp 0.48 0.010 1.000 1 2012 2012
dbSNP: rs10451941
rs10451941
1 1.000 0.036 3 193637313 intron variant T/A,C snp 0.42 0.44 0.010 1.000 1 2013 2013
dbSNP: rs10483727
rs10483727
4 0.846 0.036 14 60606157 regulatory region variant T/C snp 0.48 0.010 1.000 1 2012 2012
dbSNP: rs1063192
rs1063192
10 0.784 0.286 9 22003368 3 prime UTR variant G/A,T snp 0.69 0.010 1.000 1 2012 2012
dbSNP: rs10759930
rs10759930
1 1.000 0.036 9 117699343 intergenic variant C/T snp 0.31 0.010 1.000 1 2008 2008
dbSNP: rs12025126
rs12025126
2 0.923 0.036 1 8699495 intron variant T/C snp 0.28 0.010 < 0.001 1 2012 2012
dbSNP: rs1256031
rs1256031
9 0.821 0.143 14 64279461 intron variant G/A snp 0.57 0.010 1.000 1 2010 2010
dbSNP: rs1799983
rs1799983
138 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 0.010 1.000 1 2016 2016
dbSNP: rs1900004
rs1900004
2 0.923 0.036 10 68241124 intron variant C/T snp 0.38; 7.0E-04 0.010 1.000 1 2012 2012
dbSNP: rs1926320
rs1926320
2 0.923 0.036 13 36078480 intron variant T/C snp 0.27 0.010 < 0.001 1 2012 2012
dbSNP: rs1927914
rs1927914
3 0.878 0.143 9 117702447 intergenic variant G/A snp 0.53 0.010 1.000 1 2008 2008
dbSNP: rs199746824
rs199746824
3 0.878 0.036 1 171652139 missense variant C/G,T snp 4.0E-06; 1.6E-05 0.010 1.000 1 2001 2001
dbSNP: rs2033008
rs2033008
1 1.000 0.036 2 105886129 intron variant T/A snp 0.30 0.010 < 0.001 1 2013 2013
dbSNP: rs2149356
rs2149356
4 0.846 0.143 9 117711921 intron variant T/G snp 0.54 0.010 1.000 1 2008 2008
dbSNP: rs2234926
rs2234926
2 0.923 0.036 1 171652385 missense variant C/T snp 0.15 0.10 0.010 1.000 1 2001 2001
dbSNP: rs2234927
rs2234927
4 0.846 0.036 1 171638703 missense variant G/A,C snp 4.0E-06; 7.6E-04 8.9E-04 0.010 1.000 1 2001 2001
dbSNP: rs3213787
rs3213787
2 0.923 0.036 2 45419685 intron variant A/G snp 4.3E-02 0.010 1.000 1 2011 2011
dbSNP: rs3858145
rs3858145
3 0.878 0.036 10 68252081 intergenic variant A/G snp 0.33 0.010 1.000 1 2012 2012
dbSNP: rs4986938
rs4986938
23 0.657 0.536 14 64233098 3 prime UTR variant C/T snp 0.31 0.32 0.010 1.000 1 2010 2010
dbSNP: rs547984
rs547984
3 0.878 0.036 1 237933586 intergenic variant A/C snp 0.60 0.010 1.000 1 2017 2017