rs2277439
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs2277439(A;A) |
Make rs2277439(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 42581307 |
Gene | TNFSF11 |
is a | snp |
is | mentioned by |
dbSNP | rs2277439 |
dbSNP (classic) | rs2277439 |
ClinGen | rs2277439 |
ebi | rs2277439 |
HLI | rs2277439 |
Exac | rs2277439 |
Gnomad | rs2277439 |
Varsome | rs2277439 |
LitVar | rs2277439 |
Map | rs2277439 |
PheGenI | rs2277439 |
Biobank | rs2277439 |
1000 genomes | rs2277439 |
hgdp | rs2277439 |
ensembl | rs2277439 |
geneview | rs2277439 |
scholar | rs2277439 |
rs2277439 | |
pharmgkb | rs2277439 |
gwascentral | rs2277439 |
openSNP | rs2277439 |
23andMe | rs2277439 |
SNPshot | rs2277439 |
SNPdbe | rs2277439 |
MSV3d | rs2277439 |
GWAS Ctlg | rs2277439 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25138264] Polymorphisms in genes in the RANKL/RANK/OPG pathway are associated with bone mineral density at different skeletal sites in post-menopausal women
ClinVar | |
---|---|
Risk | rs2277439(A;A) |
Alt | rs2277439(A;A) |
Reference | Rs2277439(G;G) |
Significance | Non-pathogenic |
Disease | not specified Osteopetrosis |
Variation | info |
Gene | TNFSF11 |
CLNDBN | not specified Osteopetrosis |
Reversed | 0 |
HGVS | NC_000013.10:g.43155443G>A |
CLNSRC | |
CLNACC | RCV000175758.1, RCV000400844.1, |