rs587781815

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6	Breast cancer associated mutation
(G;G)	0	common in clinvar

Make rs587781815(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108272852

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587781815
dbSNP (classic)	rs587781815
ClinGen	rs587781815
ebi	rs587781815
HLI	rs587781815
Exac	rs587781815
Gnomad	rs587781815
Varsome	rs587781815
LitVar	rs587781815
Map	rs587781815
PheGenI	rs587781815
Biobank	rs587781815
1000 genomes	rs587781815
hgdp	rs587781815
ensembl	rs587781815
geneview	rs587781815
scholar	rs587781815
google	rs587781815
pharmgkb	rs587781815
gwascentral	rs587781815
openSNP	rs587781815
23andMe	rs587781815
SNPshot	rs587781815
SNPdbe	rs587781815
MSV3d	rs587781815
GWAS Ctlg	rs587781815

Max Magnitude

6

ClinVar
Risk	rs587781815(A;A)
Alt	rs587781815(A;A)
Reference	Rs587781815(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108143579G>A
CLNSRC
CLNACC	RCV000130088.2,