rs13091637
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13091637(C;C) |
Make rs13091637(C;T) |
Make rs13091637(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 142547597 |
Gene | ATR |
is a | snp |
is | mentioned by |
dbSNP | rs13091637 |
dbSNP (classic) | rs13091637 |
ClinGen | rs13091637 |
ebi | rs13091637 |
HLI | rs13091637 |
Exac | rs13091637 |
Gnomad | rs13091637 |
Varsome | rs13091637 |
LitVar | rs13091637 |
Map | rs13091637 |
PheGenI | rs13091637 |
Biobank | rs13091637 |
1000 genomes | rs13091637 |
hgdp | rs13091637 |
ensembl | rs13091637 |
geneview | rs13091637 |
scholar | rs13091637 |
rs13091637 | |
pharmgkb | rs13091637 |
gwascentral | rs13091637 |
openSNP | rs13091637 |
23andMe | rs13091637 |
SNPshot | rs13091637 |
SNPdbe | rs13091637 |
MSV3d | rs13091637 |
GWAS Ctlg | rs13091637 |
GMAF | 0.1497 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 20513533] Interaction between BRCA1/BRCA2 and ATM/ATR associate with breast cancer susceptibility in a Chinese Han population
[PMID 17010193] Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families.