rs2073617

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs2073617(C;T)

Make rs2073617(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

118952044

Gene	COLEC10, TNFRSF11B

is a	snp
is	mentioned by
dbSNP	rs2073617
dbSNP (classic)	rs2073617
ClinGen	rs2073617
ebi	rs2073617
HLI	rs2073617
Exac	rs2073617
Gnomad	rs2073617
Varsome	rs2073617
LitVar	rs2073617
Map	rs2073617
PheGenI	rs2073617
Biobank	rs2073617
1000 genomes	rs2073617
hgdp	rs2073617
ensembl	rs2073617
geneview	rs2073617
scholar	rs2073617
google	rs2073617
pharmgkb	rs2073617
gwascentral	rs2073617
openSNP	rs2073617
23andMe	rs2073617
SNPshot	rs2073617
SNPdbe	rs2073617
MSV3d	rs2073617
GWAS Ctlg	rs2073617

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 26065000 ] 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 28824302 ] Association of Genes Variants in RANKL/RANK/OPG Signaling Pathway with the Development of Osteonecrosis of the Femoral Head in Chinese Population.

[PMID 30309792] Association of SNP-SNP Interactions Between RANKL, OPG, CHI3L1, and VDR Genes With Breast Cancer Risk in Egyptian Women.

[PMID 31658533] [Association between TNFRSF11A and TNFRSF11B gene polymorphisms and the outcome of hepatitis C virus infection].