rs6426748
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs6426748(C;T) |
Make rs6426748(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 22381072 |
is a | snp |
is | mentioned by |
dbSNP | rs6426748 |
dbSNP (classic) | rs6426748 |
ClinGen | rs6426748 |
ebi | rs6426748 |
HLI | rs6426748 |
Exac | rs6426748 |
Gnomad | rs6426748 |
Varsome | rs6426748 |
LitVar | rs6426748 |
Map | rs6426748 |
PheGenI | rs6426748 |
Biobank | rs6426748 |
1000 genomes | rs6426748 |
hgdp | rs6426748 |
ensembl | rs6426748 |
geneview | rs6426748 |
scholar | rs6426748 |
rs6426748 | |
pharmgkb | rs6426748 |
gwascentral | rs6426748 |
openSNP | rs6426748 |
23andMe | rs6426748 |
SNPshot | rs6426748 |
SNPdbe | rs6426748 |
MSV3d | rs6426748 |
GWAS Ctlg | rs6426748 |
GMAF | 0.185 |
Max Magnitude | 0 |
? | (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]