GRM4, glutamate metabotropic receptor 4, 2914

N. diseases: 54; N. variants: 5
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: rs1906953
rs1906953 		0.882 0.040 6 34068669 intron variant C/T snv 0.25
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		Neoplasms 0.820 1.000 3 2013 2016
dbSNP: rs1906953
rs1906953 		0.882 0.040 6 34068669 intron variant C/T snv 0.25
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		Neoplasms 0.020 1.000 2 2014 2016
dbSNP: rs1906953
rs1906953 		0.882 0.040 6 34068669 intron variant C/T snv 0.25
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma 		Neoplasms 0.020 1.000 2 2014 2016
dbSNP: rs1906953
rs1906953 		0.882 0.040 6 34068669 intron variant C/T snv 0.25
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 < 0.001 1 2014 2014
dbSNP: rs2029461
rs2029461 		1.000 0.040 6 34138013 intron variant C/T snv 0.43
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy 		Nervous System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2229901
rs2229901 		1.000 0.040 6 34022670 3 prime UTR variant T/C snv 0.32
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs2499697
rs2499697 		0.925 0.040 6 34077141 intron variant A/C;G snv
CUI: C0014544
Disease: Epilepsy
Epilepsy 		Nervous System Diseases 0.010 < 0.001 1 2019 2019
dbSNP: rs2499697
rs2499697 		0.925 0.040 6 34077141 intron variant A/C;G snv
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2499707
rs2499707 		0.925 0.120 6 34085889 intron variant T/A;C snv
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2499707
rs2499707 		0.925 0.120 6 34085889 intron variant T/A;C snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2018 2018