rs876659454

Orientation

plus

Stabilized

plus

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

Make rs876659454(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108315898

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876659454
dbSNP (classic)	rs876659454
ClinGen	rs876659454
ebi	rs876659454
HLI	rs876659454
Exac	rs876659454
Gnomad	rs876659454
Varsome	rs876659454
LitVar	rs876659454
Map	rs876659454
PheGenI	rs876659454
Biobank	rs876659454
1000 genomes	rs876659454
hgdp	rs876659454
ensembl	rs876659454
geneview	rs876659454
scholar	rs876659454
google	rs876659454
pharmgkb	rs876659454
gwascentral	rs876659454
openSNP	rs876659454
23andMe	rs876659454
SNPshot	rs876659454
SNPdbe	rs876659454
MSV3d	rs876659454
GWAS Ctlg	rs876659454

Max Magnitude

6

ClinVar
Risk	rs876659454(T;T)
Alt	rs876659454(T;T)
Reference	Rs876659454(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.108186625C>T
CLNSRC
CLNACC	RCV000213485.1,