rs876660066

Orientation

plus

Stabilized

plus

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

Make rs876660066(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108347278

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876660066
dbSNP (classic)	rs876660066
ClinGen	rs876660066
ebi	rs876660066
HLI	rs876660066
Exac	rs876660066
Gnomad	rs876660066
Varsome	rs876660066
LitVar	rs876660066
Map	rs876660066
PheGenI	rs876660066
Biobank	rs876660066
1000 genomes	rs876660066
hgdp	rs876660066
ensembl	rs876660066
geneview	rs876660066
scholar	rs876660066
google	rs876660066
pharmgkb	rs876660066
gwascentral	rs876660066
openSNP	rs876660066
23andMe	rs876660066
SNPshot	rs876660066
SNPdbe	rs876660066
MSV3d	rs876660066
GWAS Ctlg	rs876660066

Max Magnitude

6

ClinVar
Risk	rs876660066(A;A)
Alt	rs876660066(A;A)
Reference	Rs876660066(G;G)
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.108218005G>A
CLNSRC
CLNACC	RCV000217583.1,