rs876658163

Orientation

plus

Stabilized

plus

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

Make rs876658163(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108320003

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876658163
dbSNP (classic)	rs876658163
ClinGen	rs876658163
ebi	rs876658163
HLI	rs876658163
Exac	rs876658163
Gnomad	rs876658163
Varsome	rs876658163
LitVar	rs876658163
Map	rs876658163
PheGenI	rs876658163
Biobank	rs876658163
1000 genomes	rs876658163
hgdp	rs876658163
ensembl	rs876658163
geneview	rs876658163
scholar	rs876658163
google	rs876658163
pharmgkb	rs876658163
gwascentral	rs876658163
openSNP	rs876658163
23andMe	rs876658163
SNPshot	rs876658163
SNPdbe	rs876658163
MSV3d	rs876658163
GWAS Ctlg	rs876658163

Max Magnitude

6

ClinVar
Risk	rs876658163(T;T)
Alt	rs876658163(T;T)
Reference	Rs876658163(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108190730C>T
CLNSRC
CLNACC	RCV000219604.1, RCV000472831.1,