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rs11155795

From SNPedia

Orientationplus
Stabilizedplus
Make rs11155795(A;A)
Make rs11155795(A;G)
Make rs11155795(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position151530204
GeneCCDC170
is asnp
is mentioned by
dbSNPrs11155795
ebirs11155795
HLIrs11155795
Exacrs11155795
Varsomers11155795
Maprs11155795
PheGenIrs11155795
hapmaprs11155795
1000 genomesrs11155795
hgdprs11155795
ensemblrs11155795
gopubmedrs11155795
geneviewrs11155795
scholarrs11155795
googlers11155795
pharmgkbrs11155795
gwascentralrs11155795
openSNPrs11155795
23andMers11155795
23andMe allrs11155795
SNP Nexus

SNPshotrs11155795
SNPdbers11155795
MSV3drs11155795
GWAS Ctlgrs11155795
GMAF0.3926
Max Magnitude
? (A;A) (A;G) (G;G) 28
Rs11155795
PubMed [PMID 18445777]
Affy Probeset SNP_A-2025991
Affy Orientation same
On GW 5.0
Alleles A/B A/G
Ancestral G
Population Caucasian
Allele G
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All -
Disease Bone mineral density, lower (BMD-L)


rs11155795 is in linkage disequilibrium with a polymorphism that increases susceptibility to Bone mineral density variations, lower for carriers of the G allele [PMID 18445777]