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rs6426748

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs6426748(C;T)
Make rs6426748(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position22381072
is asnp
is mentioned by
dbSNPrs6426748
ebirs6426748
HLIrs6426748
Exacrs6426748
Varsomers6426748
Maprs6426748
PheGenIrs6426748
hapmaprs6426748
1000 genomesrs6426748
hgdprs6426748
ensemblrs6426748
gopubmedrs6426748
geneviewrs6426748
scholarrs6426748
googlers6426748
pharmgkbrs6426748
gwascentralrs6426748
openSNPrs6426748
23andMers6426748
23andMe allrs6426748
SNP Nexus

SNPshotrs6426748
SNPdbers6426748
MSV3drs6426748
GWAS Ctlgrs6426748
GMAF0.185
Max Magnitude0
? (C;C) (C;T) (T;T) 28
Rs6426748
PubMed [PMID 18445777]
Affy Probeset SNP_A-2276784
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 -
Disease Bone mineral density, lower (BMD-L)


rs6426748 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone mineral density variations, lower for carriers of the C allele [PMID 18445777]

rs6426748 is in linkage disequilibrium with a polymorphism that increases susceptibility to Osteoporotic fractures 1.15 times for carriers of the C allele [PMID 18445777]