rs587779846

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs587779846(-;-)

Make rs587779846(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108301760

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs587779846
dbSNP (classic)	rs587779846
ClinGen	rs587779846
ebi	rs587779846
HLI	rs587779846
Exac	rs587779846
Gnomad	rs587779846
Varsome	rs587779846
LitVar	rs587779846
Map	rs587779846
PheGenI	rs587779846
Biobank	rs587779846
1000 genomes	rs587779846
hgdp	rs587779846
ensembl	rs587779846
geneview	rs587779846
scholar	rs587779846
google	rs587779846
pharmgkb	rs587779846
gwascentral	rs587779846
openSNP	rs587779846
23andMe	rs587779846
SNPshot	rs587779846
SNPdbe	rs587779846
MSV3d	rs587779846
GWAS Ctlg	rs587779846

Max Magnitude

0

ClinVar
Risk	rs587779846(-;-)
Alt	rs587779846(-;-)
Reference	Rs587779846(C;C)
Significance	Other
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.108172487delC
CLNSRC
CLNACC	RCV000115210.5, RCV000169483.3, RCV000235105.1,