rs863224440

Orientation

plus

Stabilized

plus

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

Make rs863224440(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108332899

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs863224440
dbSNP (classic)	rs863224440
ClinGen	rs863224440
ebi	rs863224440
HLI	rs863224440
Exac	rs863224440
Gnomad	rs863224440
Varsome	rs863224440
LitVar	rs863224440
Map	rs863224440
PheGenI	rs863224440
Biobank	rs863224440
1000 genomes	rs863224440
hgdp	rs863224440
ensembl	rs863224440
geneview	rs863224440
scholar	rs863224440
google	rs863224440
pharmgkb	rs863224440
gwascentral	rs863224440
openSNP	rs863224440
23andMe	rs863224440
SNPshot	rs863224440
SNPdbe	rs863224440
MSV3d	rs863224440
GWAS Ctlg	rs863224440

Max Magnitude

6

ClinVar
Risk	rs863224440(C;C)
Alt	rs863224440(C;C)
Reference	Rs863224440(A;A)
Significance	Probable-Pathogenic
Disease	Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	C11orf65 ATM
CLNDBN	Ataxia-telangiectasia syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108203626A>C
CLNSRC
CLNACC	RCV000197870.1, RCV000215938.1, RCV000420030.1,