rs587782660

Orientation

plus

Stabilized

plus

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

Make rs587782660(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108244842

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587782660
dbSNP (classic)	rs587782660
ClinGen	rs587782660
ebi	rs587782660
HLI	rs587782660
Exac	rs587782660
Gnomad	rs587782660
Varsome	rs587782660
LitVar	rs587782660
Map	rs587782660
PheGenI	rs587782660
Biobank	rs587782660
1000 genomes	rs587782660
hgdp	rs587782660
ensembl	rs587782660
geneview	rs587782660
scholar	rs587782660
google	rs587782660
pharmgkb	rs587782660
gwascentral	rs587782660
openSNP	rs587782660
23andMe	rs587782660
SNPshot	rs587782660
SNPdbe	rs587782660
MSV3d	rs587782660
GWAS Ctlg	rs587782660

Max Magnitude

6

ClinVar
Risk	rs587782660(-;-)
Alt	rs587782660(-;-)
Reference	Rs587782660(CCTC;CCTC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108115569_108115572delCCTC
CLNSRC
CLNACC	RCV000132076.4, RCV000484835.1,