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rs3793427

From SNPedia

Orientationplus
Stabilizedplus
Make rs3793427(C;C)
Make rs3793427(C;G)
Make rs3793427(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position17286321
GeneVPS37A
is asnp
is mentioned by
dbSNPrs3793427
ebirs3793427
HLIrs3793427
Exacrs3793427
Varsomers3793427
Maprs3793427
PheGenIrs3793427
hapmaprs3793427
1000 genomesrs3793427
hgdprs3793427
ensemblrs3793427
gopubmedrs3793427
geneviewrs3793427
scholarrs3793427
googlers3793427
pharmgkbrs3793427
gwascentralrs3793427
openSNPrs3793427
23andMers3793427
23andMe allrs3793427
SNP Nexus

SNPshotrs3793427
SNPdbers3793427
MSV3drs3793427
GWAS Ctlgrs3793427
GMAF0.4917
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 17903302OA-icon.png]
Trait Tonometry
Title Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
Risk Allele
P-val 0.0000019999999999999999
Odds Ratio NR NR


GET Evidence
rs3793427
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.362056
summary