rs598126
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs598126(C;C) |
Make rs598126(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 42564502 |
Gene | COASY |
is a | snp |
is | mentioned by |
dbSNP | rs598126 |
dbSNP (classic) | rs598126 |
ClinGen | rs598126 |
ebi | rs598126 |
HLI | rs598126 |
Exac | rs598126 |
Gnomad | rs598126 |
Varsome | rs598126 |
LitVar | rs598126 |
Map | rs598126 |
PheGenI | rs598126 |
Biobank | rs598126 |
1000 genomes | rs598126 |
hgdp | rs598126 |
ensembl | rs598126 |
geneview | rs598126 |
scholar | rs598126 |
rs598126 | |
pharmgkb | rs598126 |
gwascentral | rs598126 |
openSNP | rs598126 |
23andMe | rs598126 |
SNPshot | rs598126 |
SNPdbe | rs598126 |
MSV3d | rs598126 |
GWAS Ctlg | rs598126 |
GMAF | 0.4725 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21092186] Polymorphisms in genes involved in the estrogen pathway and mammographic density
[PMID 18843021] HSD17B1 genetic variants and hormone receptor-defined breast cancer.
[PMID 19015200] Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer.
ClinVar | |
---|---|
Risk | rs598126(C;C) |
Alt | rs598126(C;C) |
Reference | Rs598126(T;T) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | COASY |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000017.10:g.40716520A>G |
CLNSRC | |
CLNACC | RCV000436954.1, |