GRM8, glutamate metabotropic receptor 8, 2918

N. diseases: 56; N. variants: 13
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: rs10232276
rs10232276 		7 126943467 intron variant T/C snv 0.23
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs10487465
rs10487465 		1.000 0.080 7 127056727 intron variant T/C snv 7.9E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs12706746
rs12706746 		1.000 0.040 7 126802805 intron variant G/A snv 0.24
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		Digestive System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs17691394
rs17691394 		0.925 7 126684537 intron variant A/G snv 0.13
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2010 2010
dbSNP: rs17691394
rs17691394 		0.925 7 126684537 intron variant A/G snv 0.13
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection 		0.700 1.000 1 2010 2010
dbSNP: rs17691394
rs17691394 		0.925 7 126684537 intron variant A/G snv 0.13
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs17691394
rs17691394 		0.925 7 126684537 intron variant A/G snv 0.13
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2010 2010
dbSNP: rs17691394
rs17691394 		0.925 7 126684537 intron variant A/G snv 0.13
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2010 2010
dbSNP: rs2283093
rs2283093 		7 127081177 intron variant C/T snv 0.17
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs4141410
rs4141410 		7 127097692 intron variant A/G snv 0.46
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2299472
rs2299472 		1.000 0.040 7 126580415 intron variant C/A snv 0.30
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.020 1.000 2 2004 2014
dbSNP: rs1361995
rs1361995 		1.000 0.040 7 126732003 intron variant C/T snv 0.35
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs17862325
rs17862325 		1.000 0.080 7 127214599 intron variant A/G snv 0.21
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs2237748
rs2237748 		1.000 0.040 7 126638809 intron variant C/T snv 0.30
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2004 2004
dbSNP: rs2237781
rs2237781 		1.000 0.040 7 127034996 intron variant G/A snv 5.4E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs712723
rs712723 		1.000 0.040 7 126439090 3 prime UTR variant A/G snv 0.41 0.41
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs886003
rs886003 		1.000 0.080 7 127206962 intron variant C/T snv 0.15
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2015 2015