rs876660631

Orientation

plus

Stabilized

plus

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

Make rs876660631(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108229197

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876660631
dbSNP (classic)	rs876660631
ClinGen	rs876660631
ebi	rs876660631
HLI	rs876660631
Exac	rs876660631
Gnomad	rs876660631
Varsome	rs876660631
LitVar	rs876660631
Map	rs876660631
PheGenI	rs876660631
Biobank	rs876660631
1000 genomes	rs876660631
hgdp	rs876660631
ensembl	rs876660631
geneview	rs876660631
scholar	rs876660631
google	rs876660631
pharmgkb	rs876660631
gwascentral	rs876660631
openSNP	rs876660631
23andMe	rs876660631
SNPshot	rs876660631
SNPdbe	rs876660631
MSV3d	rs876660631
GWAS Ctlg	rs876660631

Max Magnitude

6

ClinVar
Risk	rs876660631(T;T)
Alt	rs876660631(T;T)
Reference	Rs876660631(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.108099924C>T
CLNSRC
CLNACC	RCV000213362.1,