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rs4811196

From SNPedia

Orientationplus
Stabilizedplus
Make rs4811196(A;A)
Make rs4811196(A;G)
Make rs4811196(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position37841292
GeneCTNNBL1
is asnp
is mentioned by
dbSNPrs4811196
ebirs4811196
HLIrs4811196
Exacrs4811196
Varsomers4811196
Maprs4811196
PheGenIrs4811196
hapmaprs4811196
1000 genomesrs4811196
hgdprs4811196
ensemblrs4811196
gopubmedrs4811196
geneviewrs4811196
scholarrs4811196
googlers4811196
pharmgkbrs4811196
gwascentralrs4811196
openSNPrs4811196
23andMers4811196
23andMe allrs4811196
SNP Nexus

SNPshotrs4811196
SNPdbers4811196
MSV3drs4811196
GWAS Ctlgrs4811196
GMAF0.1795
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903296OA-icon.png]
Trait Bone mineral density
Title Genome-wide association with bone mass and geometry in the Framingham Heart Study
Risk Allele
P-val 9.9999999999999995E-7
Odds Ratio NR NR

[PMID 17903301OA-icon.png] Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.


GET Evidence
rs4811196
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.804688
summary