rs587781963

Orientation

plus

Stabilized

plus

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

Make rs587781963(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108310255

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587781963
dbSNP (classic)	rs587781963
ClinGen	rs587781963
ebi	rs587781963
HLI	rs587781963
Exac	rs587781963
Gnomad	rs587781963
Varsome	rs587781963
LitVar	rs587781963
Map	rs587781963
PheGenI	rs587781963
Biobank	rs587781963
1000 genomes	rs587781963
hgdp	rs587781963
ensembl	rs587781963
geneview	rs587781963
scholar	rs587781963
google	rs587781963
pharmgkb	rs587781963
gwascentral	rs587781963
openSNP	rs587781963
23andMe	rs587781963
SNPshot	rs587781963
SNPdbe	rs587781963
MSV3d	rs587781963
GWAS Ctlg	rs587781963

Max Magnitude

6

ClinVar
Risk	rs587781963(T;T)
Alt	rs587781963(T;T)
Reference	Rs587781963(C;C)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108180982C>T
CLNSRC
CLNACC	RCV000130342.2,