APLN, apelin, 8862

N. diseases: 226; N. variants: 11
Disease: Hypertensive disease ×
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: rs3761581
rs3761581 		0.851 0.160 X 129655744 upstream gene variant A/C snv 0.11
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.040 1.000 4 2009 2016
dbSNP: rs56204867
rs56204867 		0.925 0.040 X 129656490 upstream gene variant A/G snv 0.11
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.020 0.500 2 2015 2019
dbSNP: rs5975126
rs5975126 		X 129646415 3 prime UTR variant G/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs755559514
rs755559514 		0.925 0.040 X 129648648 missense variant T/C;G snv 1.2E-05; 6.1E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs909656
rs909656 		X 129648585 intron variant G/A;T snv 1.4E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018