rs1802904
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1802904(A;A) |
Make rs1802904(A;G) |
Make rs1802904(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 142449489 |
Gene | ATR, XRN1 |
is a | snp |
is | mentioned by |
dbSNP | rs1802904 |
dbSNP (classic) | rs1802904 |
ClinGen | rs1802904 |
ebi | rs1802904 |
HLI | rs1802904 |
Exac | rs1802904 |
Gnomad | rs1802904 |
Varsome | rs1802904 |
LitVar | rs1802904 |
Map | rs1802904 |
PheGenI | rs1802904 |
Biobank | rs1802904 |
1000 genomes | rs1802904 |
hgdp | rs1802904 |
ensembl | rs1802904 |
geneview | rs1802904 |
scholar | rs1802904 |
rs1802904 | |
pharmgkb | rs1802904 |
gwascentral | rs1802904 |
openSNP | rs1802904 |
23andMe | rs1802904 |
SNPshot | rs1802904 |
SNPdbe | rs1802904 |
MSV3d | rs1802904 |
GWAS Ctlg | rs1802904 |
GMAF | 0.09734 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23844225] Associations of ATR and CHEK1 Single Nucleotide Polymorphisms with Breast Cancer
[PMID 17010193] Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families.
ClinVar | |
---|---|
Risk | rs1802904(A;A) |
Alt | rs1802904(A;A) |
Reference | rs1802904(G;G) |
Significance | Other |
Disease | not specified Seckel syndrome |
Variation | info |
Gene | XRN1 ATR |
CLNDBN | not specified Seckel syndrome |
Reversed | 1 |
HGVS | NC_000003.11:g.142168331C>T |
CLNSRC | ClinVar Emory University University of Chicago |
CLNACC | RCV000079601.6, RCV000366216.1, |