rs587782192

Orientation

plus

Stabilized

plus

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

Make rs587782192(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108284460

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587782192
dbSNP (classic)	rs587782192
ClinGen	rs587782192
ebi	rs587782192
HLI	rs587782192
Exac	rs587782192
Gnomad	rs587782192
Varsome	rs587782192
LitVar	rs587782192
Map	rs587782192
PheGenI	rs587782192
Biobank	rs587782192
1000 genomes	rs587782192
hgdp	rs587782192
ensembl	rs587782192
geneview	rs587782192
scholar	rs587782192
google	rs587782192
pharmgkb	rs587782192
gwascentral	rs587782192
openSNP	rs587782192
23andMe	rs587782192
SNPshot	rs587782192
SNPdbe	rs587782192
MSV3d	rs587782192
GWAS Ctlg	rs587782192

Max Magnitude

6

ClinVar
Risk	rs587782192(G;G)
Alt	rs587782192(G;G)
Reference	Rs587782192(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108155187T>G
CLNSRC
CLNACC	RCV000130840.3, RCV000463924.1,