rs587781545

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	Breast cancer associated mutation

Make rs587781545(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108229275

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587781545
dbSNP (classic)	rs587781545
ClinGen	rs587781545
ebi	rs587781545
HLI	rs587781545
Exac	rs587781545
Gnomad	rs587781545
Varsome	rs587781545
LitVar	rs587781545
Map	rs587781545
PheGenI	rs587781545
Biobank	rs587781545
1000 genomes	rs587781545
hgdp	rs587781545
ensembl	rs587781545
geneview	rs587781545
scholar	rs587781545
google	rs587781545
pharmgkb	rs587781545
gwascentral	rs587781545
openSNP	rs587781545
23andMe	rs587781545
SNPshot	rs587781545
SNPdbe	rs587781545
MSV3d	rs587781545
GWAS Ctlg	rs587781545

Max Magnitude

6

ClinVar
Risk	rs587781545(A;A) rs587781545(T;T)
Alt	rs587781545(A;A) rs587781545(T;T)
Reference	Rs587781545(C;C)
Significance	Pathogenic
Disease	not specified Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	not specified Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108100002C>A; NC_000011.9:g.108100002C>T
CLNSRC
CLNACC	RCV000159724.3, RCV000229615.2, RCV000445811.1, RCV000129559.3,