Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10094579
rs10094579
0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2018 2018
dbSNP: rs10204525
rs10204525
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2011 2011
dbSNP: rs10454134
rs10454134
1.000 0.200 2 48420887 TF binding site variant G/A snv 0.14
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2019 2019
dbSNP: rs1048709
rs1048709
0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2016 2016
dbSNP: rs104894559
rs104894559
CA4
0.882 0.200 17 60150074 missense variant C/T snv 2.5E-04 1.4E-04
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2008 2008
dbSNP: rs104895083
rs104895083
0.925 0.200 16 3247166 missense variant G/C;T snv 4.0E-05; 1.2E-05
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2008 2008
dbSNP: rs104895094
rs104895094
0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2006 2006
dbSNP: rs104895297
rs104895297
MVK
0.882 0.360 12 109581427 missense variant C/T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2007 2007
dbSNP: rs10499194
rs10499194
0.752 0.400 6 137681500 intron variant C/T snv 0.24
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2013 2013
dbSNP: rs10515746
rs10515746
0.925 0.240 5 157109557 intron variant A/C;T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2019 2019
dbSNP: rs1061622
rs1061622
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2003 2003
dbSNP: rs1065407
rs1065407
1.000 0.200 5 96776379 3 prime UTR variant T/A;G snv 3.3E-05; 0.26
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2015 2015
dbSNP: rs10863888
rs10863888
0.851 0.280 1 211329427 intron variant A/C;G;T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2014 2014
dbSNP: rs111874856
rs111874856
1.000 0.200 18 21028924 missense variant C/T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2014 2014
dbSNP: rs11209026
rs11209026
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2014 2014
dbSNP: rs112108028
rs112108028
1.000 0.200 18 20959861 missense variant G/A snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2014 2014
dbSNP: rs112130712
rs112130712
1.000 0.200 18 20967783 missense variant T/C snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2014 2014
dbSNP: rs11230563
rs11230563
0.790 0.360 11 61008737 missense variant C/G;T snv 4.2E-06; 0.31
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2016 2016
dbSNP: rs1126772
rs1126772
0.851 0.320 4 87983034 3 prime UTR variant A/G snv 0.16
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2011 2011
dbSNP: rs1128503
rs1128503
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2012 2012
dbSNP: rs11574944
rs11574944
1.000 0.200 16 30498669 intron variant C/T snv 0.25
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2014 2014
dbSNP: rs11614913
rs11614913
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2013 2013
dbSNP: rs11642873
rs11642873
0.851 0.280 16 85958099 intergenic variant A/C snv 0.15
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2016 2016
dbSNP: rs11755527
rs11755527
0.851 0.360 6 90248512 intron variant C/G snv 0.36
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2015 2015
dbSNP: rs11769828
rs11769828
1.000 0.200 7 150534221 intergenic variant C/T snv 0.19
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.010 1.000 1 2013 2013