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: rs7495132
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.800 1.000 2 2012 2017
dbSNP: rs10083558
rs10083558
CRTC3-AS1 ; LINC01585
15 90659273 intron variant C/A snv 0.30
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs2010672
rs2010672
CRTC3-AS1
15 90658042 intron variant G/C;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs2010672
rs2010672
CRTC3-AS1
15 90658042 intron variant G/C;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7165170
rs7165170
CRTC3 ; CRTC3-AS1
1.000 0.040 15 90638257 non coding transcript exon variant A/C snv 0.26
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs7165170
rs7165170
CRTC3 ; CRTC3-AS1
1.000 0.040 15 90638257 non coding transcript exon variant A/C snv 0.26
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs7495132
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 1 2019 2019
dbSNP: rs7495132
rs7495132
CRTC3 ; CRTC3-AS1
0.790 0.080 15 90629669 intron variant C/T snv 0.12
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.700 1.000 1 2019 2019