rs587781597

Orientation

plus

Stabilized

plus

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

Make rs587781597(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108345829

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587781597
dbSNP (classic)	rs587781597
ClinGen	rs587781597
ebi	rs587781597
HLI	rs587781597
Exac	rs587781597
Gnomad	rs587781597
Varsome	rs587781597
LitVar	rs587781597
Map	rs587781597
PheGenI	rs587781597
Biobank	rs587781597
1000 genomes	rs587781597
hgdp	rs587781597
ensembl	rs587781597
geneview	rs587781597
scholar	rs587781597
google	rs587781597
pharmgkb	rs587781597
gwascentral	rs587781597
openSNP	rs587781597
23andMe	rs587781597
SNPshot	rs587781597
SNPdbe	rs587781597
MSV3d	rs587781597
GWAS Ctlg	rs587781597

Max Magnitude

6

ClinVar
Risk	rs587781597(A;A)
Alt	rs587781597(A;A)
Reference	Rs587781597(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108216556C>A
CLNSRC
CLNACC	RCV000129661.2,