rs587779834

Orientation

plus

Stabilized

plus

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

Make rs587779834(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108284282

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587779834
dbSNP (classic)	rs587779834
ClinGen	rs587779834
ebi	rs587779834
HLI	rs587779834
Exac	rs587779834
Gnomad	rs587779834
Varsome	rs587779834
LitVar	rs587779834
Map	rs587779834
PheGenI	rs587779834
Biobank	rs587779834
1000 genomes	rs587779834
hgdp	rs587779834
ensembl	rs587779834
geneview	rs587779834
scholar	rs587779834
google	rs587779834
pharmgkb	rs587779834
gwascentral	rs587779834
openSNP	rs587779834
23andMe	rs587779834
SNPshot	rs587779834
SNPdbe	rs587779834
MSV3d	rs587779834
GWAS Ctlg	rs587779834

Merged from

Rs765158119

Max Magnitude

6

ClinVar
Risk	rs587779834(-;-)
Alt	rs587779834(-;-)
Reference	Rs587779834(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108155009delG
CLNSRC
CLNACC	RCV000115179.7, RCV000198788.4, RCV000212002.2,