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rs4959677

From SNPedia

Orientationplus
Stabilizedplus
Make rs4959677(C;C)
Make rs4959677(C;G)
Make rs4959677(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position2500586
is asnp
is mentioned by
dbSNPrs4959677
ebirs4959677
HLIrs4959677
Exacrs4959677
Varsomers4959677
Maprs4959677
PheGenIrs4959677
hapmaprs4959677
1000 genomesrs4959677
hgdprs4959677
ensemblrs4959677
gopubmedrs4959677
geneviewrs4959677
scholarrs4959677
googlers4959677
pharmgkbrs4959677
gwascentralrs4959677
openSNPrs4959677
23andMers4959677
23andMe allrs4959677
SNP Nexus

SNPshotrs4959677
SNPdbers4959677
MSV3drs4959677
GWAS Ctlgrs4959677
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 24124408OA-icon.png]
Trait Orthostatic hypotension
Title Genome-wide association study of orthostatic hypotension and supine-standing blood pressure changes in two korean populations.
Risk Allele C
P-val 9E-6
Odds Ratio .83 [NR] mmHg increase