rs876658587

Orientation

plus

Stabilized

plus

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

Make rs876658587(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108293475

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876658587
dbSNP (classic)	rs876658587
ClinGen	rs876658587
ebi	rs876658587
HLI	rs876658587
Exac	rs876658587
Gnomad	rs876658587
Varsome	rs876658587
LitVar	rs876658587
Map	rs876658587
PheGenI	rs876658587
Biobank	rs876658587
1000 genomes	rs876658587
hgdp	rs876658587
ensembl	rs876658587
geneview	rs876658587
scholar	rs876658587
google	rs876658587
pharmgkb	rs876658587
gwascentral	rs876658587
openSNP	rs876658587
23andMe	rs876658587
SNPshot	rs876658587
SNPdbe	rs876658587
MSV3d	rs876658587
GWAS Ctlg	rs876658587

Max Magnitude

6

ClinVar
Risk	rs876658587(T;T)
Alt	rs876658587(T;T)
Reference	Rs876658587(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108164202G>T
CLNSRC
CLNACC	RCV000219771.1,