rs772821016

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	Breast cancer associated mutation

Make rs772821016(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108244873

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs772821016
dbSNP (classic)	rs772821016
ClinGen	rs772821016
ebi	rs772821016
HLI	rs772821016
Exac	rs772821016
Gnomad	rs772821016
Varsome	rs772821016
LitVar	rs772821016
Map	rs772821016
PheGenI	rs772821016
Biobank	rs772821016
1000 genomes	rs772821016
hgdp	rs772821016
ensembl	rs772821016
geneview	rs772821016
scholar	rs772821016
google	rs772821016
pharmgkb	rs772821016
gwascentral	rs772821016
openSNP	rs772821016
23andMe	rs772821016
SNPshot	rs772821016
SNPdbe	rs772821016
MSV3d	rs772821016
GWAS Ctlg	rs772821016

Max Magnitude

6

ClinVar
Risk	rs772821016(T;T)
Alt	rs772821016(T;T)
Reference	Rs772821016(C;C)
Significance	Pathogenic
Disease	Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108115600C>T
CLNSRC
CLNACC	RCV000196975.2, RCV000216766.1, RCV000479464.1,