rs587781805

Orientation

plus

Stabilized

plus

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

Make rs587781805(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108271107

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587781805
dbSNP (classic)	rs587781805
ClinGen	rs587781805
ebi	rs587781805
HLI	rs587781805
Exac	rs587781805
Gnomad	rs587781805
Varsome	rs587781805
LitVar	rs587781805
Map	rs587781805
PheGenI	rs587781805
Biobank	rs587781805
1000 genomes	rs587781805
hgdp	rs587781805
ensembl	rs587781805
geneview	rs587781805
scholar	rs587781805
google	rs587781805
pharmgkb	rs587781805
gwascentral	rs587781805
openSNP	rs587781805
23andMe	rs587781805
SNPshot	rs587781805
SNPdbe	rs587781805
MSV3d	rs587781805
GWAS Ctlg	rs587781805

Max Magnitude

6

ClinVar
Risk	rs587781805(-;-)
Alt	rs587781805(-;-)
Reference	Rs587781805(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108141834delT
CLNSRC
CLNACC	RCV000130076.2,