NOS1, nitric oxide synthase 1, 4842

N. diseases: 521; N. variants: 38
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: rs28607014
rs28607014 		1.000 0.040 12 117270806 intron variant C/T snv 0.32
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 2 2017 2019
dbSNP: rs73208120
rs73208120 		0.790 0.080 12 117309785 intron variant T/G snv 7.1E-02
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		0.700 1.000 2 2015 2019
dbSNP: rs73208120
rs73208120 		0.790 0.080 12 117309785 intron variant T/G snv 7.1E-02
CUI: C0346629
Disease: Malignant neoplasm of large intestine
Malignant neoplasm of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2015 2019
dbSNP: rs73208120
rs73208120 		0.790 0.080 12 117309785 intron variant T/G snv 7.1E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2015 2019
dbSNP: rs73208120
rs73208120 		0.790 0.080 12 117309785 intron variant T/G snv 7.1E-02
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2015 2019
dbSNP: rs73208120
rs73208120 		0.790 0.080 12 117309785 intron variant T/G snv 7.1E-02
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		0.700 1.000 2 2015 2019
dbSNP: rs73208120
rs73208120 		0.790 0.080 12 117309785 intron variant T/G snv 7.1E-02
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		0.700 1.000 2 2015 2019
dbSNP: rs73208120
rs73208120 		0.790 0.080 12 117309785 intron variant T/G snv 7.1E-02
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2015 2019
dbSNP: rs73208120
rs73208120 		0.790 0.080 12 117309785 intron variant T/G snv 7.1E-02
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		0.700 1.000 2 2015 2019
dbSNP: rs73208120
rs73208120 		0.790 0.080 12 117309785 intron variant T/G snv 7.1E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		Digestive System Diseases; Neoplasms 0.700 1.000 2 2015 2019
dbSNP: rs2291909
rs2291909 		12 117247112 intron variant T/G snv 3.4E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2291909
rs2291909 		12 117247112 intron variant T/G snv 3.4E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2293052
rs2293052 		1.000 0.040 12 117277815 intron variant G/A snv 0.28
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs76830467
rs76830467 		1.000 0.080 12 117321510 intron variant A/T snv 3.4E-02
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs76830467
rs76830467 		1.000 0.080 12 117321510 intron variant A/T snv 3.4E-02
CUI: C0201968
Disease: Cortisol Measurement
Cortisol Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7960451
rs7960451 		12 117235437 intron variant C/T snv 8.0E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7960451
rs7960451 		12 117235437 intron variant C/T snv 8.0E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9658292
rs9658292 		12 117318980 intron variant G/C snv 9.4E-04
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9658292
rs9658292 		12 117318980 intron variant G/C snv 9.4E-04
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9658292
rs9658292 		12 117318980 intron variant G/C snv 9.4E-04
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9658292
rs9658292 		12 117318980 intron variant G/C snv 9.4E-04
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9658292
rs9658292 		12 117318980 intron variant G/C snv 9.4E-04
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9658449
rs9658449 		12 117252327 intron variant A/G snv 3.3E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9658449
rs9658449 		12 117252327 intron variant A/G snv 3.3E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs9658465
rs9658465 		12 117247093 intron variant T/G snv 2.3E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012