RGS5, regulator of G protein signaling 5, 8490

N. diseases: 52; 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: rs76121963
rs76121963 		1 163269560 intron variant T/G snv 2.6E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs902727464
rs902727464 		1 163221517 intron variant TCAATAAA/- delins 9.3E-05
CUI: C0948364
Disease: Periprosthetic osteolysis
Periprosthetic osteolysis 		Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1056515
rs1056515 		0.882 0.040 1 163143470 3 prime UTR variant G/T snv 0.37
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1056515
rs1056515 		0.882 0.040 1 163143470 3 prime UTR variant G/T snv 0.37
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1056515
rs1056515 		0.882 0.040 1 163143470 3 prime UTR variant G/T snv 0.37
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs16849802
rs16849802 		1.000 0.040 1 163145396 3 prime UTR variant G/A snv 4.4E-03
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs16849802
rs16849802 		1.000 0.040 1 163145396 3 prime UTR variant G/A snv 4.4E-03
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2815272
rs2815272 		1 163203457 intron variant G/C snv 5.4E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2011 2011