PCNX1, pecanex 1, 22990

N. diseases: 12; N. variants: 5
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: rs143046984
rs143046984
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.710 1.000 1 2016 2016
dbSNP: rs2526882
rs2526882
1.000 0.040 14 70907985 synonymous variant G/A;C snv 0.62
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 2 2017 2019
dbSNP: rs67981189
rs67981189
1.000 0.040 14 71005509 intron variant A/G snv 0.36
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 2 2015 2019
dbSNP: rs143046984
rs143046984
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs143046984
rs143046984
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2016 2016
dbSNP: rs143046984
rs143046984
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2016 2016
dbSNP: rs143046984
rs143046984
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02
Malignant neoplasm of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs143046984
rs143046984
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2016 2016
dbSNP: rs143046984
rs143046984
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs143046984
rs143046984
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs143046984
rs143046984
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2016 2016
dbSNP: rs2286313
rs2286313
0.790 0.080 14 71047446 intron variant A/G snv 4.0E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs2286313
rs2286313
0.790 0.080 14 71047446 intron variant A/G snv 4.0E-02
Malignant neoplasm of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs2286313
rs2286313
0.790 0.080 14 71047446 intron variant A/G snv 4.0E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2016 2016
dbSNP: rs2286313
rs2286313
0.790 0.080 14 71047446 intron variant A/G snv 4.0E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs2286313
rs2286313
0.790 0.080 14 71047446 intron variant A/G snv 4.0E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2016 2016
dbSNP: rs2286313
rs2286313
0.790 0.080 14 71047446 intron variant A/G snv 4.0E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2016 2016
dbSNP: rs2286313
rs2286313
0.790 0.080 14 71047446 intron variant A/G snv 4.0E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs2286313
rs2286313
0.790 0.080 14 71047446 intron variant A/G snv 4.0E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs2286313
rs2286313
0.790 0.080 14 71047446 intron variant A/G snv 4.0E-02
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2016 2016
dbSNP: rs2526882
rs2526882
1.000 0.040 14 70907985 synonymous variant G/A;C snv 0.62
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs7154284
rs7154284
14 70990265 intron variant A/T snv 2.3E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019