rs587781752

Orientation

plus

Stabilized

plus

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

Make rs587781752(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108279575

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587781752
dbSNP (classic)	rs587781752
ClinGen	rs587781752
ebi	rs587781752
HLI	rs587781752
Exac	rs587781752
Gnomad	rs587781752
Varsome	rs587781752
LitVar	rs587781752
Map	rs587781752
PheGenI	rs587781752
Biobank	rs587781752
1000 genomes	rs587781752
hgdp	rs587781752
ensembl	rs587781752
geneview	rs587781752
scholar	rs587781752
google	rs587781752
pharmgkb	rs587781752
gwascentral	rs587781752
openSNP	rs587781752
23andMe	rs587781752
SNPshot	rs587781752
SNPdbe	rs587781752
MSV3d	rs587781752
GWAS Ctlg	rs587781752

Max Magnitude

6

ClinVar
Risk	rs587781752(-;-)
Alt	rs587781752(-;-)
Reference	Rs587781752(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108150302delA
CLNSRC
CLNACC	RCV000129958.2,