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rs4373814

From SNPedia

Orientationplus
Stabilizedplus
Make rs4373814(C;C)
Make rs4373814(C;G)
Make rs4373814(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position18131043
is asnp
is mentioned by
dbSNPrs4373814
ebirs4373814
HLIrs4373814
Exacrs4373814
Varsomers4373814
Maprs4373814
PheGenIrs4373814
hapmaprs4373814
1000 genomesrs4373814
hgdprs4373814
ensemblrs4373814
gopubmedrs4373814
geneviewrs4373814
scholarrs4373814
googlers4373814
pharmgkbrs4373814
gwascentralrs4373814
openSNPrs4373814
23andMers4373814
23andMe allrs4373814
SNP Nexus

SNPshotrs4373814
SNPdbers4373814
MSV3drs4373814
GWAS Ctlgrs4373814
GMAF0.4853
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21909115OA-icon.png]
Trait
Title Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Risk Allele G
P-val 4E-10
Odds Ratio 0.2180 [NR] mmHg decrease

[PMID 24338417] Genetic variations in MOV10 and CACNB2 are associated with hypertension in a Chinese Han population