HCRTR2, hypocretin receptor 2, 3062

N. diseases: 37; N. variants: 11
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: rs9367630
rs9367630 		1.000 6 55283305 downstream gene variant G/A snv 3.2E-02
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 1.000 1 2009 2009
dbSNP: rs9367630
rs9367630 		1.000 6 55283305 downstream gene variant G/A snv 3.2E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 1 2009 2009
dbSNP: rs9367630
rs9367630 		1.000 6 55283305 downstream gene variant G/A snv 3.2E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.800 1.000 1 2009 2009
dbSNP: rs9367630
rs9367630 		1.000 6 55283305 downstream gene variant G/A snv 3.2E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 1 2009 2009
dbSNP: rs3122163
rs3122163 		6 55191570 intron variant C/T snv 0.85
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		0.700 1.000 1 2017 2017
dbSNP: rs3122163
rs3122163 		6 55191570 intron variant C/T snv 0.85
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2017 2017
dbSNP: rs35833281
rs35833281 		6 55156763 intron variant G/C snv 0.15
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		0.700 1.000 1 2016 2016
dbSNP: rs4454139
rs4454139 		6 55178438 intron variant A/C;T snv
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement 		0.700 1.000 1 2019 2019
dbSNP: rs76899638
rs76899638 		6 55282710 downstream gene variant -/GT delins 0.83
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		0.700 1.000 1 2016 2016
dbSNP: rs9367621
rs9367621 		6 55175492 intron variant T/A snv 0.61
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs2653349
rs2653349 		0.882 0.120 6 55277539 missense variant A/G;T snv 0.84; 4.0E-06
CUI: C0009088
Disease: Cluster Headache
Cluster Headache 		Nervous System Diseases 0.050 0.400 5 2015 2020
dbSNP: rs2134294
rs2134294 		1.000 0.080 6 55269449 intron variant T/C snv 0.47
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs2653342
rs2653342 		1.000 0.040 6 55266339 intron variant A/G snv 0.89
CUI: C0009088
Disease: Cluster Headache
Cluster Headache 		Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2653349
rs2653349 		0.882 0.120 6 55277539 missense variant A/G;T snv 0.84; 4.0E-06
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs2653349
rs2653349 		0.882 0.120 6 55277539 missense variant A/G;T snv 0.84; 4.0E-06
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 < 0.001 1 2019 2019
dbSNP: rs2653349
rs2653349 		0.882 0.120 6 55277539 missense variant A/G;T snv 0.84; 4.0E-06
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2015 2015
dbSNP: rs2653349
rs2653349 		0.882 0.120 6 55277539 missense variant A/G;T snv 0.84; 4.0E-06
CUI: C0018021
Disease: Goiter
Goiter 		Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3122156
rs3122156 		1.000 0.040 6 55218009 intron variant T/G snv 0.36
CUI: C0009088
Disease: Cluster Headache
Cluster Headache 		Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs9370399
rs9370399 		1.000 0.080 6 55180227 intron variant A/C;G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2016 2016