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rs1561570

From SNPedia

Orientationplus
Stabilizedplus
Make rs1561570(C;C)
Make rs1561570(C;T)
Make rs1561570(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position13113726
GeneOPTN
is asnp
is mentioned by
dbSNPrs1561570
ebirs1561570
HLIrs1561570
Exacrs1561570
Varsomers1561570
Maprs1561570
PheGenIrs1561570
hapmaprs1561570
1000 genomesrs1561570
hgdprs1561570
ensemblrs1561570
gopubmedrs1561570
geneviewrs1561570
scholarrs1561570
googlers1561570
pharmgkbrs1561570
gwascentralrs1561570
openSNPrs1561570
23andMers1561570
23andMe allrs1561570
SNP Nexus

SNPshotrs1561570
SNPdbers1561570
MSV3drs1561570
GWAS Ctlgrs1561570
GMAF0.4518
Max Magnitude
? (C;C) (C;T) (T;T) 28
related to Paget’s disease of bone 23andMe blog.
GWAS snp
PMID [PMID 20436471OA-icon.png]
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]
OMIM602080
Desc
Variant
Relatedalso
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 22796589OA-icon.png] Genetic association study of UCMA/GRP and OPTN genes (PDB6 locus) with Paget's disease of bone.