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rs6959212

From SNPedia

Orientationplus
Stabilizedplus
Make rs6959212(C;C)
Make rs6959212(C;T)
Make rs6959212(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position38088724
is asnp
is mentioned by
dbSNPrs6959212
ebirs6959212
HLIrs6959212
Exacrs6959212
Varsomers6959212
Maprs6959212
PheGenIrs6959212
hapmaprs6959212
1000 genomesrs6959212
hgdprs6959212
ensemblrs6959212
gopubmedrs6959212
geneviewrs6959212
scholarrs6959212
googlers6959212
pharmgkbrs6959212
gwascentralrs6959212
openSNPrs6959212
23andMers6959212
23andMe allrs6959212
SNP Nexus

SNPshotrs6959212
SNPdbers6959212
MSV3drs6959212
GWAS Ctlgrs6959212
GMAF0.3517
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22504420OA-icon.png]
Trait
Title Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
Risk Allele T
P-val 4E-38
Odds Ratio 0.0700 None
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 2E-9
Odds Ratio .02 [NR] unit decrease