AGTR1, angiotensin II receptor type 1, 185

N. diseases: 440; N. variants: 33
Disease: Essential Hypertension ×
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: rs5186
rs5186 		0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.030 1.000 3 2014 2018
dbSNP: rs5182
rs5182 		0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.020 0.500 2 1994 2018
dbSNP: rs12695895
rs12695895 		0.925 0.040 3 148725481 intron variant C/T snv 0.31
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2638360
rs2638360 		0.925 0.080 3 148710569 intron variant G/A;T snv
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs387967
rs387967 		1.000 0.040 3 148697698 upstream gene variant G/C snv 0.20
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs777986489
rs777986489 		1.000 0.040 3 148741657 missense variant T/C snv 3.2E-05 2.8E-05
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2004 2004
dbSNP: rs911154679
rs911154679 		1.000 0.040 3 148741352 missense variant C/T snv 7.0E-06
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2010 2010