rs587782863

Orientation

plus

Stabilized

plus

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

Make rs587782863(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108289724

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587782863
dbSNP (classic)	rs587782863
ClinGen	rs587782863
ebi	rs587782863
HLI	rs587782863
Exac	rs587782863
Gnomad	rs587782863
Varsome	rs587782863
LitVar	rs587782863
Map	rs587782863
PheGenI	rs587782863
Biobank	rs587782863
1000 genomes	rs587782863
hgdp	rs587782863
ensembl	rs587782863
geneview	rs587782863
scholar	rs587782863
google	rs587782863
pharmgkb	rs587782863
gwascentral	rs587782863
openSNP	rs587782863
23andMe	rs587782863
SNPshot	rs587782863
SNPdbe	rs587782863
MSV3d	rs587782863
GWAS Ctlg	rs587782863

Max Magnitude

6

ClinVar
Risk	rs587782863(-;-)
Alt	rs587782863(-;-)
Reference	Rs587782863(AAAAA;AAAAA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.108160451_108160455delAAAAA
CLNSRC
CLNACC	RCV000132482.2,