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rs4131805

From SNPedia

Orientationminus
Stabilizedminus
Make rs4131805(A;A)
Make rs4131805(A;G)
Make rs4131805(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position28479148
is asnp
is mentioned by
dbSNPrs4131805
ebirs4131805
HLIrs4131805
Exacrs4131805
Varsomers4131805
Maprs4131805
PheGenIrs4131805
hapmaprs4131805
1000 genomesrs4131805
hgdprs4131805
ensemblrs4131805
gopubmedrs4131805
geneviewrs4131805
scholarrs4131805
googlers4131805
pharmgkbrs4131805
gwascentralrs4131805
openSNPrs4131805
23andMers4131805
23andMe allrs4131805
SNP Nexus

SNPshotrs4131805
SNPdbers4131805
MSV3drs4131805
GWAS Ctlgrs4131805
GMAF0.3035
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 0.0000019999999999999999
Odds Ratio NR NR


GET Evidence
rs4131805
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.359375
summary