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rs10770612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs10770612(A;G)
Make rs10770612(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position20077705
GeneLOC100506393
is asnp
is mentioned by
dbSNPrs10770612
dbSNP (classic)rs10770612
ClinGenrs10770612
ebirs10770612
HLIrs10770612
Exacrs10770612
Gnomadrs10770612
Varsomers10770612
LitVarrs10770612
Maprs10770612
PheGenIrs10770612
Biobankrs10770612
1000 genomesrs10770612
hgdprs10770612
ensemblrs10770612
geneviewrs10770612
scholarrs10770612
googlers10770612
pharmgkbrs10770612
gwascentralrs10770612
openSNPrs10770612
23andMers10770612
SNPshotrs10770612
SNPdbers10770612
MSV3drs10770612
GWAS Ctlgrs10770612
GMAF0.2016
Max Magnitude0
? (A;A) (A;G) (G;G) 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 G
P-val 2E-8
Odds Ratio 0.03 [0.02-0.04] cm increase