rs587781776

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs587781776(-;-)

Make rs587781776(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108250820

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587781776
dbSNP (classic)	rs587781776
ClinGen	rs587781776
ebi	rs587781776
HLI	rs587781776
Exac	rs587781776
Gnomad	rs587781776
Varsome	rs587781776
LitVar	rs587781776
Map	rs587781776
PheGenI	rs587781776
Biobank	rs587781776
1000 genomes	rs587781776
hgdp	rs587781776
ensembl	rs587781776
geneview	rs587781776
scholar	rs587781776
google	rs587781776
pharmgkb	rs587781776
gwascentral	rs587781776
openSNP	rs587781776
23andMe	rs587781776
SNPshot	rs587781776
SNPdbe	rs587781776
MSV3d	rs587781776
GWAS Ctlg	rs587781776

Max Magnitude

0

ClinVar
Risk	rs587781776(-;-)
Alt	rs587781776(-;-)
Reference	Rs587781776(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108121547delC
CLNSRC
CLNACC	RCV000130017.2, RCV000466554.1,