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rs4715166

From SNPedia

Orientationplus
Stabilizedplus
Make rs4715166(A;A)
Make rs4715166(A;G)
Make rs4715166(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position13215826
GenePHACTR1
is asnp
is mentioned by
dbSNPrs4715166
ebirs4715166
HLIrs4715166
Exacrs4715166
Varsomers4715166
Maprs4715166
PheGenIrs4715166
hapmaprs4715166
1000 genomesrs4715166
hgdprs4715166
ensemblrs4715166
gopubmedrs4715166
geneviewrs4715166
scholarrs4715166
googlers4715166
pharmgkbrs4715166
gwascentralrs4715166
openSNPrs4715166
23andMers4715166
23andMe allrs4715166
SNP Nexus

SNPshotrs4715166
SNPdbers4715166
MSV3drs4715166
GWAS Ctlgrs4715166
GMAF0.4803
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 17903296OA-icon.png]
Trait Hip geometry
Title Genome-wide association with bone mass and geometry in the Framingham Heart Study
Risk Allele
P-val 0.0000030000000000000001
Odds Ratio NR NR


[PMID 17903299OA-icon.png] A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.


GET Evidence
rs4715166
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.460938
summary