RGS7, regulator of G protein signaling 7, 6000

N. diseases: 28; N. variants: 25
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: rs10802916
rs10802916 		1.000 0.040 1 240968716 intron variant T/A snv 0.39
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10926380
rs10926380 		1.000 0.040 1 240928436 intron variant C/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11586002
rs11586002 		1.000 0.040 1 240970404 intron variant T/C snv 0.36
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs116135446
rs116135446 		1 240794633 intron variant C/T snv 2.6E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs12038552
rs12038552 		1.000 0.040 1 240943761 intron variant C/T snv 0.35
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12119557
rs12119557 		1.000 0.040 1 240968001 intron variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs146390073
rs146390073 		1.000 1 241142948 intron variant C/T snv 1.1E-02
CUI: C1531624
Disease: Cardioembolic stroke
Cardioembolic stroke 		0.700 1.000 1 2018 2018
dbSNP: rs16840647
rs16840647 		1.000 0.120 1 240799770 intron variant A/G snv 4.1E-02
CUI: C0022336
Disease: Creutzfeldt-Jakob disease
Creutzfeldt-Jakob disease 		Infections; Nervous System Diseases; Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs16841100
rs16841100 		1.000 0.040 1 240942759 intron variant C/T snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs16841101
rs16841101 		1.000 0.040 1 240943470 intron variant A/T snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs16841106
rs16841106 		1.000 0.040 1 240943626 intron variant G/C snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs16841107
rs16841107 		1.000 0.040 1 240943819 intron variant T/C snv 8.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1915872
rs1915872 		1 241198493 intron variant G/A snv 0.20
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2017 2017
dbSNP: rs1996806
rs1996806 		1.000 0.040 1 241270165 intron variant C/T snv 0.25
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2502439
rs2502439 		1.000 0.040 1 240959861 intron variant G/A snv 9.7E-03
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs2616968
rs2616968 		1.000 0.040 1 240958458 intron variant C/T snv 0.14
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs4659585
rs4659585 		1.000 0.040 1 240972210 intron variant C/A snv 0.41
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs4659586
rs4659586 		1.000 0.040 1 240976392 intron variant A/T snv 0.91
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs4660051
rs4660051 		1.000 0.040 1 241270547 intron variant C/T snv 0.53
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6682594
rs6682594 		1.000 0.040 1 240942171 intron variant C/T snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6690744
rs6690744 		1.000 0.040 1 240970260 intron variant T/G snv 0.41
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs679992
rs679992 		1.000 0.080 1 241024982 intron variant C/T snv 0.45
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs11805657
rs11805657 		1.000 0.040 1 240955726 intron variant T/C snv 0.87
CUI: C0030319
Disease: Panic Disorder
Panic Disorder 		Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs746273282
rs746273282 		1.000 0.040 1 240806162 missense variant C/T snv 8.0E-06 7.0E-06
CUI: C0025202
Disease: melanoma
melanoma 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs755007339
rs755007339 		1.000 0.040 1 241098711 missense variant G/A;C snv 1.2E-05; 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2018 2018