Source: GWASCAT

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: rs27524
rs27524
CAST ; ERAP1
0.851 0.160 5 96766240 intron variant A/G snv 0.61
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.800 1.000 2 2010 2015
dbSNP: rs27033
rs27033
CAST ; ERAP1
5 96771195 intron variant T/A snv 0.52
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs27044
rs27044
ERAP1 ; LOC102724748
0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.710 1.000 1 2015 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 1 2013 2019
dbSNP: rs17482078
rs17482078
ERAP1 ; LOC102724748
0.882 0.240 5 96783162 missense variant C/G;T snv 2.8E-05; 0.15
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs27432
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		0.700 1.000 1 2015 2015
dbSNP: rs27432
rs27432
ERAP1 ; LOC102724748
0.925 0.040 5 96783569 intron variant A/C;G snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.800 1.000 1 2012 2012
dbSNP: rs39841
rs39841
ERAP1 ; LOC102724748
1.000 0.040 5 96784466 intron variant G/A;C snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs42398
rs42398
ERAP1 ; LOC102724748
5 96784751 intron variant C/T snv 0.80
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2032890
rs2032890
ERAP1 ; LOC102724748
1.000 0.040 5 96785448 non coding transcript exon variant A/C;T snv
CUI: C0042165
Disease: Anterior uveitis
Anterior uveitis 		0.700 1.000 1 2015 2015
dbSNP: rs469758
rs469758
ERAP1 ; LOC102724748
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs469758
rs469758
ERAP1 ; LOC102724748
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs469758
rs469758
ERAP1 ; LOC102724748
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs469758
rs469758
ERAP1 ; LOC102724748
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs469758
rs469758
ERAP1 ; LOC102724748
0.827 0.120 5 96786011 intron variant C/T snv 0.62 0.63
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs397964890
rs397964890
ERAP1
5 96787817 intron variant -/AT;ATAT delins 0.63
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs30187
rs30187
ERAP1
0.732 0.360 5 96788627 missense variant T/A;C snv 0.62
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.900 0.957 2 2009 2020
dbSNP: rs27529
rs27529
ERAP1
1.000 0.040 5 96790605 missense variant A/G;T snv 0.62
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.710 1.000 1 2011 2019
dbSNP: rs27434
rs27434
ERAP1
1.000 0.040 5 96793809 synonymous variant A/G;T snv 0.72; 1.2E-05
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.890 1.000 1 2009 2018
dbSNP: rs202110856
rs202110856
ERAP1
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
ERAP1
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
ERAP1
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
ERAP1
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
ERAP1
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2015 2015
dbSNP: rs202110856
rs202110856
ERAP1
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2015 2015