rs587782085

Orientation

plus

Stabilized

plus

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

Make rs587782085(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108249025

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587782085
dbSNP (classic)	rs587782085
ClinGen	rs587782085
ebi	rs587782085
HLI	rs587782085
Exac	rs587782085
Gnomad	rs587782085
Varsome	rs587782085
LitVar	rs587782085
Map	rs587782085
PheGenI	rs587782085
Biobank	rs587782085
1000 genomes	rs587782085
hgdp	rs587782085
ensembl	rs587782085
geneview	rs587782085
scholar	rs587782085
google	rs587782085
pharmgkb	rs587782085
gwascentral	rs587782085
openSNP	rs587782085
23andMe	rs587782085
SNPshot	rs587782085
SNPdbe	rs587782085
MSV3d	rs587782085
GWAS Ctlg	rs587782085

Max Magnitude

6

ClinVar
Risk	rs587782085(-;-)
Alt	rs587782085(-;-)
Reference	Rs587782085(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108119752delG
CLNSRC
CLNACC	RCV000130585.2, RCV000486071.1,