rs587781449

Orientation

plus

Stabilized

plus

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

Make rs587781449(-;-)

Make rs587781449(-;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108235716

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587781449
dbSNP (classic)	rs587781449
ClinGen	rs587781449
ebi	rs587781449
HLI	rs587781449
Exac	rs587781449
Gnomad	rs587781449
Varsome	rs587781449
LitVar	rs587781449
Map	rs587781449
PheGenI	rs587781449
Biobank	rs587781449
1000 genomes	rs587781449
hgdp	rs587781449
ensembl	rs587781449
geneview	rs587781449
scholar	rs587781449
google	rs587781449
pharmgkb	rs587781449
gwascentral	rs587781449
openSNP	rs587781449
23andMe	rs587781449
SNPshot	rs587781449
SNPdbe	rs587781449
MSV3d	rs587781449
GWAS Ctlg	rs587781449

Max Magnitude

0

ClinVar
Risk	rs587781449(-;-)
Alt	rs587781449(-;-)
Reference	Rs587781449(T;T)
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.108106443delT
CLNSRC
CLNACC	RCV000129372.3, RCV000464543.1,