rs587781722

Orientation

plus

Stabilized

plus

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

Make rs587781722(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108310305

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587781722
dbSNP (classic)	rs587781722
ClinGen	rs587781722
ebi	rs587781722
HLI	rs587781722
Exac	rs587781722
Gnomad	rs587781722
Varsome	rs587781722
LitVar	rs587781722
Map	rs587781722
PheGenI	rs587781722
Biobank	rs587781722
1000 genomes	rs587781722
hgdp	rs587781722
ensembl	rs587781722
geneview	rs587781722
scholar	rs587781722
google	rs587781722
pharmgkb	rs587781722
gwascentral	rs587781722
openSNP	rs587781722
23andMe	rs587781722
SNPshot	rs587781722
SNPdbe	rs587781722
MSV3d	rs587781722
GWAS Ctlg	rs587781722

Max Magnitude

6

ClinVar
Risk	rs587781722(T;T)
Alt	rs587781722(T;T)
Reference	Rs587781722(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108181032C>T
CLNSRC
CLNACC	RCV000129909.3, RCV000200350.2, RCV000235704.2,