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rs4026608

From SNPedia

Orientationplus
Stabilizedplus
Make rs4026608(C;C)
Make rs4026608(C;T)
Make rs4026608(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position66000884
is asnp
is mentioned by
dbSNPrs4026608
ebirs4026608
HLIrs4026608
Exacrs4026608
Varsomers4026608
Maprs4026608
PheGenIrs4026608
hapmaprs4026608
1000 genomesrs4026608
hgdprs4026608
ensemblrs4026608
gopubmedrs4026608
geneviewrs4026608
scholarrs4026608
googlers4026608
pharmgkbrs4026608
gwascentralrs4026608
openSNPrs4026608
23andMers4026608
23andMe allrs4026608
SNP Nexus

SNPshotrs4026608
SNPdbers4026608
MSV3drs4026608
GWAS Ctlgrs4026608
GMAF0.4844
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19584346OA-icon.png]
Trait Aortic root size
Title Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data
Risk Allele C
P-val 2E-9
Odds Ratio 0.03 [0.02-0.04] cm decrease


GET Evidence
rs4026608
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.585938
summary