rs587782114

Orientation

plus

Stabilized

plus

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

Make rs587782114(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108317500

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587782114
dbSNP (classic)	rs587782114
ClinGen	rs587782114
ebi	rs587782114
HLI	rs587782114
Exac	rs587782114
Gnomad	rs587782114
Varsome	rs587782114
LitVar	rs587782114
Map	rs587782114
PheGenI	rs587782114
Biobank	rs587782114
1000 genomes	rs587782114
hgdp	rs587782114
ensembl	rs587782114
geneview	rs587782114
scholar	rs587782114
google	rs587782114
pharmgkb	rs587782114
gwascentral	rs587782114
openSNP	rs587782114
23andMe	rs587782114
SNPshot	rs587782114
SNPdbe	rs587782114
MSV3d	rs587782114
GWAS Ctlg	rs587782114

Max Magnitude

6

ClinVar
Risk	rs587782114(A;A)
Alt	rs587782114(A;A)
Reference	Rs587782114(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108188227G>A
CLNSRC
CLNACC	RCV000130633.2,