rs3092856

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs3092856(C;T)

Make rs3092856(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

108289005

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs3092856
dbSNP (classic)	rs3092856
ClinGen	rs3092856
ebi	rs3092856
HLI	rs3092856
Exac	rs3092856
Gnomad	rs3092856
Varsome	rs3092856
LitVar	rs3092856
Map	rs3092856
PheGenI	rs3092856
Biobank	rs3092856
1000 genomes	rs3092856
hgdp	rs3092856
ensembl	rs3092856
geneview	rs3092856
scholar	rs3092856
google	rs3092856
pharmgkb	rs3092856
gwascentral	rs3092856
openSNP	rs3092856
23andMe	rs3092856
SNPshot	rs3092856
SNPdbe	rs3092856
MSV3d	rs3092856
GWAS Ctlg	rs3092856

GMAF

0.01974

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

This SNP, a variant in the ATM gene, is 1 of 25 SNPs reported to represent independently minor, but cumulatively significant, increased risk for breast cancer. [PMID 17341484]

For details of all 25 SNPs in this group, along with the two methods used to calculate overall risk estimates for breast cancer, refer to the SNPedia breast cancer entry.

For this particular SNP, the risk (minor) allele is (T).

[PMID 20232390] Genetic variations of DNA repair genes and their prognostic significance in patients with acute myeloid leukemia

[PMID 18638378 ] Analysis of variants in DNA damage signalling genes in bladder cancer.

ClinVar
Risk	rs3092856(T;T)
Alt	rs3092856(T;T)
Reference	Rs3092856(C;C)
Significance	Other
Disease	not specified Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	not specified Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108159732C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000120137.3, RCV000128897.2, RCV000284881.1,