TACR1, tachykinin receptor 1, 6869

N. diseases: 217; N. variants: 10
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: rs1106854
rs1106854 		0.827 0.080 2 75050887 intron variant T/C;G snv
CUI: C1970945
Disease: MAJOR AFFECTIVE DISORDER 6
MAJOR AFFECTIVE DISORDER 6 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs1106854
rs1106854 		0.827 0.080 2 75050887 intron variant T/C;G snv
CUI: C1852197
Disease: MAJOR AFFECTIVE DISORDER 1
MAJOR AFFECTIVE DISORDER 1 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs1106854
rs1106854 		0.827 0.080 2 75050887 intron variant T/C;G snv
CUI: C1839839
Disease: MAJOR AFFECTIVE DISORDER 2
MAJOR AFFECTIVE DISORDER 2 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs1106854
rs1106854 		0.827 0.080 2 75050887 intron variant T/C;G snv
CUI: C1970943
Disease: MAJOR AFFECTIVE DISORDER 4
MAJOR AFFECTIVE DISORDER 4 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs1106854
rs1106854 		0.827 0.080 2 75050887 intron variant T/C;G snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs11688000
rs11688000 		1.000 0.040 2 75066030 intron variant A/G snv 0.34
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		Musculoskeletal Diseases 0.010 1.000 1 2017 2017
dbSNP: rs12477554
rs12477554 		0.925 0.080 2 75174939 intron variant A/G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs12477554
rs12477554 		0.925 0.080 2 75174939 intron variant A/G;T snv
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2012 2012
dbSNP: rs3755457
rs3755457 		0.925 0.080 2 75064383 intron variant G/A snv 0.28
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs3755457
rs3755457 		0.925 0.080 2 75064383 intron variant G/A snv 0.28
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2012 2012
dbSNP: rs3755468
rs3755468 		2 75155265 intron variant T/C snv 0.59
CUI: C0520909
Disease: Postoperative Nausea and Vomiting
Postoperative Nausea and Vomiting 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2015 2015
dbSNP: rs3771829
rs3771829 		0.790 0.120 2 75137019 intron variant C/G snv 0.11
CUI: C1839839
Disease: MAJOR AFFECTIVE DISORDER 2
MAJOR AFFECTIVE DISORDER 2 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs3771829
rs3771829 		0.790 0.120 2 75137019 intron variant C/G snv 0.11
CUI: C0004936
Disease: Mental disorders
Mental disorders 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs3771829
rs3771829 		0.790 0.120 2 75137019 intron variant C/G snv 0.11
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs3771829
rs3771829 		0.790 0.120 2 75137019 intron variant C/G snv 0.11
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs3771829
rs3771829 		0.790 0.120 2 75137019 intron variant C/G snv 0.11
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs3771829
rs3771829 		0.790 0.120 2 75137019 intron variant C/G snv 0.11
CUI: C1852197
Disease: MAJOR AFFECTIVE DISORDER 1
MAJOR AFFECTIVE DISORDER 1 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs3771829
rs3771829 		0.790 0.120 2 75137019 intron variant C/G snv 0.11
CUI: C1970943
Disease: MAJOR AFFECTIVE DISORDER 4
MAJOR AFFECTIVE DISORDER 4 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs3771829
rs3771829 		0.790 0.120 2 75137019 intron variant C/G snv 0.11
CUI: C1970945
Disease: MAJOR AFFECTIVE DISORDER 6
MAJOR AFFECTIVE DISORDER 6 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs3771829
rs3771829 		0.790 0.120 2 75137019 intron variant C/G snv 0.11
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs3771856
rs3771856 		0.882 0.080 2 75186888 non coding transcript exon variant G/A snv 0.57
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs3771856
rs3771856 		0.882 0.080 2 75186888 non coding transcript exon variant G/A snv 0.57
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs3771856
rs3771856 		0.882 0.080 2 75186888 non coding transcript exon variant G/A snv 0.57
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs3771863
rs3771863 		0.925 0.240 2 75192588 intron variant C/T snv 0.30
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia 		Musculoskeletal Diseases; Nervous System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3771863
rs3771863 		0.925 0.240 2 75192588 intron variant C/T snv 0.30
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome 		Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.010 1.000 1 2015 2015