rs2296239
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2296239(C;T) |
Make rs2296239(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 54158989 |
Gene | CYP24A1 |
is a | snp |
is | mentioned by |
dbSNP | rs2296239 |
dbSNP (classic) | rs2296239 |
ClinGen | rs2296239 |
ebi | rs2296239 |
HLI | rs2296239 |
Exac | rs2296239 |
Gnomad | rs2296239 |
Varsome | rs2296239 |
LitVar | rs2296239 |
Map | rs2296239 |
PheGenI | rs2296239 |
Biobank | rs2296239 |
1000 genomes | rs2296239 |
hgdp | rs2296239 |
ensembl | rs2296239 |
geneview | rs2296239 |
scholar | rs2296239 |
rs2296239 | |
pharmgkb | rs2296239 |
gwascentral | rs2296239 |
openSNP | rs2296239 |
23andMe | rs2296239 |
SNPshot | rs2296239 |
SNPdbe | rs2296239 |
MSV3d | rs2296239 |
GWAS Ctlg | rs2296239 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23381556] Genetic association analysis of vitamin D pathway with obesity traits
ClinVar | |
---|---|
Risk | rs2296239(T;T) |
Alt | rs2296239(T;T) |
Reference | Rs2296239(C;C) |
Significance | Non-pathogenic |
Disease | Infantile hypercalcemia |
Variation | info |
Gene | CYP24A1 |
CLNDBN | Infantile hypercalcemia |
Reversed | 0 |
HGVS | NC_000020.10:g.52775528C>T |
CLNSRC | |
CLNACC | RCV000262895.1, |