HCRTR1, hypocretin receptor 1, 3061

N. diseases: 71; N. variants: 6
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: rs10798879
rs10798879 		1 31631214 intron variant T/C snv 0.55
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs10798880
rs10798880 		1 31631487 intron variant G/A;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2017 2017
dbSNP: rs10914457
rs10914457 		1 31628660 intron variant C/A snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs2271933
rs2271933 		0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.020 1.000 2 2005 2007
dbSNP: rs2271933
rs2271933 		0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.020 1.000 2 2018 2019
dbSNP: rs10914456
rs10914456 		1.000 0.040 1 31622570 intron variant T/C snv 0.51
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		Behavior and Behavior Mechanisms 0.010 1.000 1 2019 2019
dbSNP: rs10914456
rs10914456 		1.000 0.040 1 31622570 intron variant T/C snv 0.51
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs2271933
rs2271933 		0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50
CUI: C0030319
Disease: Panic Disorder
Panic Disorder 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs2271933
rs2271933 		0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs2271933
rs2271933 		0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50
CUI: C0001818
Disease: Agoraphobia
Agoraphobia 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs2271933
rs2271933 		0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50
CUI: C0085602
Disease: Polydipsia
Polydipsia 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2007 2007
dbSNP: rs2271933
rs2271933 		0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50
CUI: C0338480
Disease: Common Migraine
Common Migraine 		Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2271933
rs2271933 		0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs2271933
rs2271933 		0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs41263963
rs41263963 		1 31627009 3 prime UTR variant G/A snv 6.1E-02 8.5E-02
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.010 1.000 1 2018 2018