rs1057516876

Orientation

plus

Stabilized

plus

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

Make rs1057516876(-;-)

Make rs1057516876(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108251884

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs1057516876
dbSNP (classic)	rs1057516876
ClinGen	rs1057516876
ebi	rs1057516876
HLI	rs1057516876
Exac	rs1057516876
Gnomad	rs1057516876
Varsome	rs1057516876
LitVar	rs1057516876
Map	rs1057516876
PheGenI	rs1057516876
Biobank	rs1057516876
1000 genomes	rs1057516876
hgdp	rs1057516876
ensembl	rs1057516876
geneview	rs1057516876
scholar	rs1057516876
google	rs1057516876
pharmgkb	rs1057516876
gwascentral	rs1057516876
openSNP	rs1057516876
23andMe	rs1057516876
SNPshot	rs1057516876
SNPdbe	rs1057516876
MSV3d	rs1057516876
GWAS Ctlg	rs1057516876

Max Magnitude

0

ClinVar
Risk	rs1057516876(-;-)
Alt	rs1057516876(-;-)
Reference	Rs1057516876(C;C)
Significance	Probable-Pathogenic
Disease	Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108122611delC
CLNSRC
CLNACC	RCV000411653.1,