rs796051858

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6	Breast cancer associated mutation
(G;G)	0	common in clinvar

Make rs796051858(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108235839

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs796051858
dbSNP (classic)	rs796051858
ClinGen	rs796051858
ebi	rs796051858
HLI	rs796051858
Exac	rs796051858
Gnomad	rs796051858
Varsome	rs796051858
LitVar	rs796051858
Map	rs796051858
PheGenI	rs796051858
Biobank	rs796051858
1000 genomes	rs796051858
hgdp	rs796051858
ensembl	rs796051858
geneview	rs796051858
scholar	rs796051858
google	rs796051858
pharmgkb	rs796051858
gwascentral	rs796051858
openSNP	rs796051858
23andMe	rs796051858
SNPshot	rs796051858
SNPdbe	rs796051858
MSV3d	rs796051858
GWAS Ctlg	rs796051858

Max Magnitude

6

ClinVar
Risk	rs796051858(A;A)
Alt	rs796051858(A;A)
Reference	Rs796051858(G;G)
Significance	Pathogenic
Disease	Ataxia-telangiectasia variant Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia variant Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108106566G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003188.4, RCV000213739.2, RCV000235952.1,