rs2586494
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2586494(A;A) |
Make rs2586494(A;C) |
Make rs2586494(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 50195794 |
Gene | COL1A1 |
is a | snp |
is | mentioned by |
dbSNP | rs2586494 |
dbSNP (classic) | rs2586494 |
ClinGen | rs2586494 |
ebi | rs2586494 |
HLI | rs2586494 |
Exac | rs2586494 |
Gnomad | rs2586494 |
Varsome | rs2586494 |
LitVar | rs2586494 |
Map | rs2586494 |
PheGenI | rs2586494 |
Biobank | rs2586494 |
1000 genomes | rs2586494 |
hgdp | rs2586494 |
ensembl | rs2586494 |
geneview | rs2586494 |
scholar | rs2586494 |
rs2586494 | |
pharmgkb | rs2586494 |
gwascentral | rs2586494 |
openSNP | rs2586494 |
23andMe | rs2586494 |
SNPshot | rs2586494 |
SNPdbe | rs2586494 |
MSV3d | rs2586494 |
GWAS Ctlg | rs2586494 |
GMAF | 0.258 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 21602843] No association between polymorphisms and haplotypes of COL1A1 and COL1A2 genes and osteoporotic fracture in postmenopausal Chinese women
[PMID 18996919] Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships.