rs876660780

Orientation

plus

Stabilized

plus

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

Make rs876660780(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108268443

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876660780
dbSNP (classic)	rs876660780
ClinGen	rs876660780
ebi	rs876660780
HLI	rs876660780
Exac	rs876660780
Gnomad	rs876660780
Varsome	rs876660780
LitVar	rs876660780
Map	rs876660780
PheGenI	rs876660780
Biobank	rs876660780
1000 genomes	rs876660780
hgdp	rs876660780
ensembl	rs876660780
geneview	rs876660780
scholar	rs876660780
google	rs876660780
pharmgkb	rs876660780
gwascentral	rs876660780
openSNP	rs876660780
23andMe	rs876660780
SNPshot	rs876660780
SNPdbe	rs876660780
MSV3d	rs876660780
GWAS Ctlg	rs876660780

Max Magnitude

6

ClinVar
Risk	rs876660780(G;G)
Alt	rs876660780(G;G)
Reference	Rs876660780(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108139170C>G
CLNSRC
CLNACC	RCV000218040.1,