GRM5, glutamate metabotropic receptor 5, 2915

N. diseases: 189; N. variants: 37
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: rs16914280
rs16914280 		1.000 11 88588556 intron variant C/T snv 4.7E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.800 1.000 1 2009 2009
dbSNP: rs16914280
rs16914280 		1.000 11 88588556 intron variant C/T snv 4.7E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 1 2009 2009
dbSNP: rs16914280
rs16914280 		1.000 11 88588556 intron variant C/T snv 4.7E-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: rs16914280
rs16914280 		1.000 11 88588556 intron variant C/T snv 4.7E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 1 2009 2009
dbSNP: rs5016282
rs5016282 		1.000 0.040 11 89008492 intron variant A/G snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.800 1.000 1 2011 2011
dbSNP: rs1553132
rs1553132 		11 88564572 intron variant A/G;T snv
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 2 2019 2019
dbSNP: rs10501678
rs10501678 		1.000 11 88708934 intron variant C/T snv 3.1E-02
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2009 2009
dbSNP: rs10501678
rs10501678 		1.000 11 88708934 intron variant C/T snv 3.1E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2009 2009
dbSNP: rs10501678
rs10501678 		1.000 11 88708934 intron variant C/T snv 3.1E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2009 2009
dbSNP: rs10501678
rs10501678 		1.000 11 88708934 intron variant C/T snv 3.1E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2009 2009
dbSNP: rs10501696
rs10501696 		1.000 0.040 11 89014994 intron variant A/G snv 0.42
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs10741500
rs10741500 		11 88703041 intron variant A/T snv 0.78
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10831496
rs10831496 		11 88824823 intron variant A/G snv 0.49
CUI: C0406208
Disease: Suntan
Suntan 		0.700 1.000 1 2009 2009
dbSNP: rs11020496
rs11020496 		0.925 0.040 11 88576138 intron variant C/A;T snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs11020496
rs11020496 		0.925 0.040 11 88576138 intron variant C/A;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1150313
rs1150313 		1.000 0.040 11 88962678 intron variant A/G snv 0.46
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs12273907
rs12273907 		1.000 0.080 11 88519531 intron variant G/A snv 0.15
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs12792431
rs12792431 		11 88687669 intron variant G/C snv 0.15
CUI: C0406208
Disease: Suntan
Suntan 		0.700 1.000 1 2018 2018
dbSNP: rs1353802
rs1353802 		11 88697984 intron variant T/C snv 0.19
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs1353804
rs1353804 		11 88702412 intron variant G/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs1353806
rs1353806 		11 88705358 intron variant C/A;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs1391874
rs1391874 		11 88702571 intron variant G/A snv 0.78
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs148065054
rs148065054 		11 88819465 intron variant C/T snv 1.7E-02
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs1499032
rs1499032 		11 88705730 intron variant C/T snv 0.78
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs1499035
rs1499035 		11 88704921 intron variant T/G snv 0.78
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013