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: rs924080
rs924080 		0.882 0.240 1 67294457 intergenic variant T/C snv 0.45
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.840 0.800 5 2010 2019
dbSNP: rs1800871
rs1800871
IL10 ; IL19
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.830 0.800 5 2010 2017
dbSNP: rs1518111
rs1518111
IL10 ; IL19
0.790 0.360 1 206771300 intron variant T/C snv 0.71
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.830 1.000 4 2010 2015
dbSNP: rs1495965
rs1495965 		0.790 0.280 1 67287825 intergenic variant C/T snv 0.55
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.820 1.000 3 2010 2017
dbSNP: rs17482078
rs17482078
ERAP1 ; LOC102724748
0.882 0.240 5 96783162 missense variant C/G;T snv 2.8E-05; 0.15
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.820 1.000 3 2013 2019
dbSNP: rs2617170
rs2617170
KLRC4 ; KLRC4-KLRK1
1.000 0.200 12 10408358 missense variant T/C snv 0.63 0.61
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.820 1.000 3 2013 2017
dbSNP: rs17810546
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.810 1.000 3 2013 2015
dbSNP: rs7574070
rs7574070
STAT4
1.000 0.200 2 191145762 intron variant A/C snv 0.55
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.810 1.000 3 2012 2015
dbSNP: rs7616215
rs7616215
CCR3 ; LOC105377067
0.925 0.280 3 46164194 intron variant C/T snv 0.62
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.810 1.000 2 2013 2015
dbSNP: rs4947296
rs4947296 		0.851 0.440 6 31090401 intergenic variant T/A;C snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 1.000 2 2012 2013
dbSNP: rs4959053
rs4959053
PSORS1C1
0.925 0.280 6 31131800 intron variant G/A snv 6.3E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 1.000 2 2012 2013
dbSNP: rs9266406
rs9266406 		1.000 0.200 6 31368641 intron variant G/A snv 0.22
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 1.000 2 2012 2013
dbSNP: rs17006292
rs17006292
TFCP2L1
1.000 0.200 2 121261187 intron variant C/A snv 2.8E-02
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 1.000 1 2012 2012
dbSNP: rs7572482
rs7572482
STAT4
1.000 0.200 2 191150346 intron variant A/C;G snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 1.000 1 2012 2012
dbSNP: rs897200
rs897200
STAT4
0.851 0.280 2 191153045 upstream gene variant T/C snv 0.54
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 1.000 1 2012 2012
dbSNP: rs3024490
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.710 0.500 2 2013 2017
dbSNP: rs1608157
rs1608157
LOC107986860
1.000 0.200 7 150549936 intergenic variant C/G;T snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.710 1.000 1 2013 2013
dbSNP: rs2253907
rs2253907 		0.882 0.360 6 31369093 intron variant C/T snv 0.43
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 1.000 2 2012 2013
dbSNP: rs9266409
rs9266409 		0.925 0.200 6 31368791 intron variant T/C snv 0.22
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 1.000 2 2012 2013
dbSNP: rs10236188
rs10236188 		1.000 0.200 7 150548168 intergenic variant T/C snv 0.49
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 1.000 1 2013 2013
dbSNP: rs10256482
rs10256482 		1.000 0.200 7 150653887 intergenic variant T/C snv 0.47
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 1.000 1 2013 2013
dbSNP: rs10277380
rs10277380 		1.000 0.200 7 150533604 intergenic variant T/A;C snv
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 1.000 1 2013 2013
dbSNP: rs1522596
rs1522596 		1.000 0.200 7 150538695 downstream gene variant A/G snv 0.47
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 1.000 1 2013 2013
dbSNP: rs1874886
rs1874886
IL12A-AS1
0.925 0.280 3 160011868 non coding transcript exon variant G/A snv 0.41
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 1.000 1 2016 2016
dbSNP: rs1916012
rs1916012 		1.000 0.200 7 150536739 intergenic variant A/G snv 0.49
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 1.000 1 2013 2013