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rs4670779

From SNPedia

Orientationplus
Stabilizedplus
Make rs4670779(C;C)
Make rs4670779(C;T)
Make rs4670779(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position37817201
GeneLOC344382
is asnp
is mentioned by
dbSNPrs4670779
ebirs4670779
HLIrs4670779
Exacrs4670779
Varsomers4670779
Maprs4670779
PheGenIrs4670779
hapmaprs4670779
1000 genomesrs4670779
hgdprs4670779
ensemblrs4670779
gopubmedrs4670779
geneviewrs4670779
scholarrs4670779
googlers4670779
pharmgkbrs4670779
gwascentralrs4670779
openSNPrs4670779
23andMers4670779
23andMe allrs4670779
SNP Nexus

SNPshotrs4670779
SNPdbers4670779
MSV3drs4670779
GWAS Ctlgrs4670779
GMAF0.2167
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19079262]
Trait Bone mineral density (spine)
Title New sequence variants associated with bone mineral density
Risk Allele T
P-val 0.000004
Odds Ratio 0.07 [0.04-0.10] SD decrease



GET Evidence
rs4670779
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary