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rs4548577

From SNPedia

Orientationplus
Stabilizedplus
Make rs4548577(C;C)
Make rs4548577(C;T)
Make rs4548577(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position46976961
GeneC11orf49
is asnp
is mentioned by
dbSNPrs4548577
ebirs4548577
HLIrs4548577
Exacrs4548577
Varsomers4548577
Maprs4548577
PheGenIrs4548577
hapmaprs4548577
1000 genomesrs4548577
hgdprs4548577
ensemblrs4548577
gopubmedrs4548577
geneviewrs4548577
scholarrs4548577
googlers4548577
pharmgkbrs4548577
gwascentralrs4548577
openSNPrs4548577
23andMers4548577
23andMe allrs4548577
SNP Nexus

SNPshotrs4548577
SNPdbers4548577
MSV3drs4548577
GWAS Ctlgrs4548577
GMAF0.314
Max Magnitude
? (C;C) (C;T) (T;T) 28
Rs4548577
PubMed [PMID 18445777]
Affy Probeset SNP_A-2158992
Affy Orientation same
On GW 5.0
Alleles A/B C/T
Ancestral C
Population Caucasian
Allele C
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.08
Disease Osteoporotic fractures (OP-F)


rs4548577 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteoporotic fractures 1.08 times for carriers of the C allele [PMID 18445777]