rs1801726
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1801726(C;C) |
Make rs1801726(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 122284985 |
Gene | CASR |
is a | snp |
is | mentioned by |
dbSNP | rs1801726 |
dbSNP (classic) | rs1801726 |
ClinGen | rs1801726 |
ebi | rs1801726 |
HLI | rs1801726 |
Exac | rs1801726 |
Gnomad | rs1801726 |
Varsome | rs1801726 |
LitVar | rs1801726 |
Map | rs1801726 |
PheGenI | rs1801726 |
Biobank | rs1801726 |
1000 genomes | rs1801726 |
hgdp | rs1801726 |
ensembl | rs1801726 |
geneview | rs1801726 |
scholar | rs1801726 |
rs1801726 | |
pharmgkb | rs1801726 |
gwascentral | rs1801726 |
openSNP | rs1801726 |
23andMe | rs1801726 |
SNPshot | rs1801726 |
SNPdbe | rs1801726 |
MSV3d | rs1801726 |
GWAS Ctlg | rs1801726 |
GMAF | 0.07668 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 20558521] Genetic variation in the retinoid X receptor and calcium-sensing receptor, and risk of colorectal cancer in the Colon Cancer Family Registry
[PMID 18787887] Genetic variation in candidate osteoporosis genes, bone mineral density, and fracture risk: the study of osteoporotic fractures.
[PMID 18843020] Genetic variation in calcium-sensing receptor and risk for colon cancer.
[PMID 23533647] Polymorphisms in the calcium-sensing receptor gene are associated with clinical outcome of neuroblastoma
[PMID 23125333] Common genetic variation of the calcium-sensing receptor and lethal prostate cancer risk.
ClinVar | |
---|---|
Risk | rs1801726(C;C) |
Alt | rs1801726(C;C) |
Reference | Rs1801726(G;G) |
Significance | Non-pathogenic |
Disease | Hypocalcemia Hypocalciuric hypercalcemia not specified |
Variation | info |
Gene | CASR |
CLNDBN | Hypocalcemia, autosomal dominant 1 Hypocalciuric hypercalcemia, familial, type 1 not specified |
Reversed | 0 |
HGVS | NC_000003.11:g.122003832G\x3d; NC_000003.11:g.122003832G>C |
CLNSRC | |
CLNACC | RCV000229426.2, RCV000152934.3, |
[PMID 29682741] Calcium-sensing receptor gene polymorphism (rs7652589) is associated with calcium nephrolithiasis in the population of Yi nationality in Southwestern China.