CBLN2, cerebellin 2 precursor, 147381

N. diseases: 19; N. variants: 2
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs658995
rs658995
1.000 0.040 18 72540105 non coding transcript exon variant A/G;T snv
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 1 2019 2019
dbSNP: rs658995
rs658995
1.000 0.040 18 72540105 non coding transcript exon variant A/G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
Nutritional and Metabolic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs694339
rs694339
0.790 0.080 18 72554745 intron variant A/G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs694339
rs694339
0.790 0.080 18 72554745 intron variant A/G;T snv
Malignant neoplasm of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs694339
rs694339
0.790 0.080 18 72554745 intron variant A/G;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2017 2017
dbSNP: rs694339
rs694339
0.790 0.080 18 72554745 intron variant A/G;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2017 2017
dbSNP: rs694339
rs694339
0.790 0.080 18 72554745 intron variant A/G;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
Digestive System Diseases; Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs694339
rs694339
0.790 0.080 18 72554745 intron variant A/G;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2017 2017
dbSNP: rs694339
rs694339
0.790 0.080 18 72554745 intron variant A/G;T snv
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs694339
rs694339
0.790 0.080 18 72554745 intron variant A/G;T snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs694339
rs694339
0.790 0.080 18 72554745 intron variant A/G;T snv
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2017 2017