SNP

dbSNP ID	Chromosome	Position	Ref allele	Alt allele	Gene

Ancestry

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Reported disease/trait	Mapped disease/Trait	Effect size	Standard error	Odds ratio	P value	Ancestry	Study
Systolic blood pressure	Systolic blood pressure	-0.0159	0.00285	0.984	7.1e-09	European	GCST90029011
Systolic blood pressure	Systolic blood pressure	-0.0159	0.00285	0.984	7.1e-09	European	GCST90029011
Systolic blood pressure	Systolic blood pressure	-0.0121	0.00221	0.988	4.56e-08	European	GCST90000062
Systolic blood pressure	Systolic blood pressure	-0.0121	0.00221	0.988	4.56e-08	European	GCST90000062
Systolic blood pressure	Systolic blood pressure	0.242	0.0424	1.27	1.17e-08	European	GCST006624
Systolic blood pressure	Systolic blood pressure	0.242	0.0424	1.27	1.17e-08	European	GCST006624

Showing 1 to 6 of 6 entries

Ancestry

Gene	Disease/Trait	Tissue	Best coloc SNP	GWAS risk SNP	SNP.PP.H4	PP.H4.abf	Ancestry	Dataset

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Reported disease	Mapped disease	Description	PMID
Acute coronary syndrome	Acute coronary syndrome	OR: 1.9; P value: <0.001; Beta: 0.64; SE: NA; Ancestry: Caucasian	22575314
Acute coronary syndrome	Acute coronary syndrome	OR: 1.9; P value: <0.001; Beta: 0.64; SE: NA; Ancestry: Caucasian	22575314

Showing 1 to 2 of 2 entries

Link to pharmGKB: https://www.pharmgkb.org/

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Reported disease	Mapped disease	Evidence	PKPD	PMID	Link
No data available in table

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Link to PedAM: http://www.unimd.org/pedam/

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Reported disease	Mapped disease	Gene	Description	PMID
Coronary artery disease	Coronary artery disease	ACCS	The MA of rs5065 ANP gene variant associates with increased susceptibility to ACS and has unfavorable prognostic value in CAD.	22575314
Coronary artery disease	Coronary artery disease	NPPA	The MA of rs5065 ANP gene variant associates with increased susceptibility to ACS and has unfavorable prognostic value in CAD.	22575314
Coronary artery disease	Coronary artery disease	NPPA	In the present study, we aimed to evaluate the potential association between one of the introduced ANP gene polymorphisms of 2238 T/C (rs5065) with coronary artery disease (CAD) in an Iranian population.	24487939
Hypertension	Hypertension	NPPA	Minor alleles of NPPA rs5068, rs5065 and rs198358 were associated with less history of hypertension; minor alleles of NPPA rs5068 and rs198358 was also associated with higher circulating natriuretic peptide levels (p=0.003 to p=0.04).	21276798
Hypertension	Hypertension	NPPA	Two common single nucleotide polymorphisms (SNPs) in NPPA, rs5063 and rs5065, result in amino acid changes of the primary peptide and have been previously implicated in conditions associated with AF, including stroke and hypertension.	20543198
Ischemic stroke	Ischemic stroke	NPPA	However, in logistic analysis for Trial of Org 10172 in Acute Stroke Treatment (TOAST) classification of ischemic stroke, nonsynonymous rs5065 (STOP152Arg) and rs5067 in 3'UTR of NPPA, which were in complete linkage disequilibrium, showed significant associations with cardioembolic stroke.	22400494

Showing 1 to 6 of 6 entries

Link to miRNASNPv3: http://bioinfo.life.hust.edu.cn/miRNASNP#!/

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Disease	Pre miRNA	Region	Mature miRNA	△G	Exp	PMID	Database
No data available in table

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Tissue	Gene	TSS distance	Effect size	Standard error	Nomimal p value	Beta p value

Basic information

GWAS significance

Colocalization analysis

Variant-disease association

GTEx eQTL