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rs4370013

From SNPedia

Orientationplus
Stabilizedplus
Make rs4370013(A;A)
Make rs4370013(A;T)
Make rs4370013(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position2613007
GeneCNTN4
is asnp
is mentioned by
dbSNPrs4370013
ebirs4370013
HLIrs4370013
Exacrs4370013
Varsomers4370013
Maprs4370013
PheGenIrs4370013
hapmaprs4370013
1000 genomesrs4370013
hgdprs4370013
ensemblrs4370013
gopubmedrs4370013
geneviewrs4370013
scholarrs4370013
googlers4370013
pharmgkbrs4370013
gwascentralrs4370013
openSNPrs4370013
23andMers4370013
23andMe allrs4370013
SNP Nexus

SNPshotrs4370013
SNPdbers4370013
MSV3drs4370013
GWAS Ctlgrs4370013
GMAF0.2213
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 17903302OA-icon.png]
Trait Blood pressure
Title Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness
Risk Allele
P-val 0.0000039999999999999998
Odds Ratio NR NR

[PMID 17903302OA-icon.png] diastolic blood pressure


GET Evidence
rs4370013
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.328125
summary