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rs2073617

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2073617(C;T)
Make rs2073617(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position118952044
GeneCOLEC10, TNFRSF11B
is asnp
is mentioned by
dbSNPrs2073617
dbSNP (old)rs2073617
ClinGenrs2073617
ebirs2073617
HLIrs2073617
Exacrs2073617
Gnomadrs2073617
Varsomers2073617
Maprs2073617
PheGenIrs2073617
Biobankrs2073617
1000 genomesrs2073617
hgdprs2073617
ensemblrs2073617
gopubmedrs2073617
geneviewrs2073617
scholarrs2073617
googlers2073617
pharmgkbrs2073617
gwascentralrs2073617
openSNPrs2073617
23andMers2073617
23andMe allrs2073617
SNP Nexus

SNPshotrs2073617
SNPdbers2073617
MSV3drs2073617
GWAS Ctlgrs2073617
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 26065000OA-icon.png] Osteoprotegerin Polymorphisms in a Mexican Population with Rheumatoid Arthritis and Generalized Osteoporosis: A Preliminary Report


[PMID 28244588] Investigation of OPG/RANK/RANKL Genes as a Genetic Marker for Cardiac abnormalities in Thalassemia Major Patients.


ClinVar
Risk rs2073617(T;T)
Alt rs2073617(T;T)
Reference Rs2073617(C;C)
Significance Non-pathogenic
Disease Hyperphosphatasemia with bone disease
Variation info
Gene TNFRSF11B COLEC10
CLNDBN Hyperphosphatasemia with bone disease
Reversed 1
HGVS NC_000008.10:g.119964283G>A
CLNSRC
CLNACC RCV000404609.1,



[PMID 28824302OA-icon.png] Association of Genes Variants in RANKL/RANK/OPG Signaling Pathway with the Development of Osteonecrosis of the Femoral Head in Chinese Population.