rs1561570
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1561570(C;C) |
Make rs1561570(C;T) |
Make rs1561570(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 13113726 |
Gene | OPTN |
is a | snp |
is | mentioned by |
dbSNP | rs1561570 |
dbSNP (classic) | rs1561570 |
ClinGen | rs1561570 |
ebi | rs1561570 |
HLI | rs1561570 |
Exac | rs1561570 |
Gnomad | rs1561570 |
Varsome | rs1561570 |
LitVar | rs1561570 |
Map | rs1561570 |
PheGenI | rs1561570 |
Biobank | rs1561570 |
1000 genomes | rs1561570 |
hgdp | rs1561570 |
ensembl | rs1561570 |
geneview | rs1561570 |
scholar | rs1561570 |
rs1561570 | |
pharmgkb | rs1561570 |
gwascentral | rs1561570 |
openSNP | rs1561570 |
23andMe | rs1561570 |
SNPshot | rs1561570 |
SNPdbe | rs1561570 |
MSV3d | rs1561570 |
GWAS Ctlg | rs1561570 |
GMAF | 0.4518 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
related to Paget’s disease of bone 23andMe blog.
GWAS snp | |
---|---|
PMID | [PMID 20436471] |
Trait | Paget's disease |
Title | Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone |
Risk Allele | |
P-val | 6E-13 |
Odds Ratio | 1.54 [1.37-1.72] |
GWAS snp | |
---|---|
PMID | [PMID 21623375] |
Trait | |
Title | Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. |
Risk Allele | T |
P-val | 4E-38 |
Odds Ratio | 1.6700 [1.54-1.80] |
[PMID 22796589] Genetic association study of UCMA/GRP and OPTN genes (PDB6 locus) with Paget's disease of bone.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 10
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d