rs876658899

Orientation

plus

Stabilized

plus

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

Make rs876658899(-;A)

Make rs876658899(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108281102

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876658899
dbSNP (classic)	rs876658899
ClinGen	rs876658899
ebi	rs876658899
HLI	rs876658899
Exac	rs876658899
Gnomad	rs876658899
Varsome	rs876658899
LitVar	rs876658899
Map	rs876658899
PheGenI	rs876658899
Biobank	rs876658899
1000 genomes	rs876658899
hgdp	rs876658899
ensembl	rs876658899
geneview	rs876658899
scholar	rs876658899
google	rs876658899
pharmgkb	rs876658899
gwascentral	rs876658899
openSNP	rs876658899
23andMe	rs876658899
SNPshot	rs876658899
SNPdbe	rs876658899
MSV3d	rs876658899
GWAS Ctlg	rs876658899

Max Magnitude

0

ClinVar
Risk	rs876658899(A;A)
Alt	rs876658899(A;A)
Reference	Rs876658899(-;-)
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.108151829dupA
CLNSRC
CLNACC	RCV000222552.1, RCV000462687.1,