rs876659283

Orientation

plus

Stabilized

plus

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

Make rs876659283(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108251997

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876659283
dbSNP (classic)	rs876659283
ClinGen	rs876659283
ebi	rs876659283
HLI	rs876659283
Exac	rs876659283
Gnomad	rs876659283
Varsome	rs876659283
LitVar	rs876659283
Map	rs876659283
PheGenI	rs876659283
Biobank	rs876659283
1000 genomes	rs876659283
hgdp	rs876659283
ensembl	rs876659283
geneview	rs876659283
scholar	rs876659283
google	rs876659283
pharmgkb	rs876659283
gwascentral	rs876659283
openSNP	rs876659283
23andMe	rs876659283
SNPshot	rs876659283
SNPdbe	rs876659283
MSV3d	rs876659283
GWAS Ctlg	rs876659283

Max Magnitude

6

ClinVar
Risk	rs876659283(T;T)
Alt	rs876659283(T;T)
Reference	Rs876659283(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.108122724G>T
CLNSRC
CLNACC	RCV000220061.1,