rs876659003

Orientation

plus

Stabilized

plus

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

Make rs876659003(-;-)

Make rs876659003(-;TG)

Make rs876659003(TG;TG)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108244881

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876659003
dbSNP (classic)	rs876659003
ClinGen	rs876659003
ebi	rs876659003
HLI	rs876659003
Exac	rs876659003
Gnomad	rs876659003
Varsome	rs876659003
LitVar	rs876659003
Map	rs876659003
PheGenI	rs876659003
Biobank	rs876659003
1000 genomes	rs876659003
hgdp	rs876659003
ensembl	rs876659003
geneview	rs876659003
scholar	rs876659003
google	rs876659003
pharmgkb	rs876659003
gwascentral	rs876659003
openSNP	rs876659003
23andMe	rs876659003
SNPshot	rs876659003
SNPdbe	rs876659003
MSV3d	rs876659003
GWAS Ctlg	rs876659003

Max Magnitude

0

ClinVar
Risk	rs876659003(-;-)
Alt	rs876659003(-;-)
Reference	Rs876659003(GT;GT)
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.108115608_108115609delTG
CLNSRC
CLNACC	RCV000222737.1, RCV000409635.1,