rs876658287

Orientation

plus

Stabilized

plus

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

Make rs876658287(-;-)

Make rs876658287(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108304727

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876658287
dbSNP (classic)	rs876658287
ClinGen	rs876658287
ebi	rs876658287
HLI	rs876658287
Exac	rs876658287
Gnomad	rs876658287
Varsome	rs876658287
LitVar	rs876658287
Map	rs876658287
PheGenI	rs876658287
Biobank	rs876658287
1000 genomes	rs876658287
hgdp	rs876658287
ensembl	rs876658287
geneview	rs876658287
scholar	rs876658287
google	rs876658287
pharmgkb	rs876658287
gwascentral	rs876658287
openSNP	rs876658287
23andMe	rs876658287
SNPshot	rs876658287
SNPdbe	rs876658287
MSV3d	rs876658287
GWAS Ctlg	rs876658287

Merged from

Rs750992549

Max Magnitude

0

ClinVar
Risk	rs876658287(-;-)
Alt	rs876658287(-;-)
Reference	Rs876658287(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome not provided Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108175454delT
CLNSRC
CLNACC	RCV000219889.1, RCV000236989.1, RCV000411540.1,