rs1057517358

Orientation

plus

Stabilized

plus

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

Make rs1057517358(A;G)

Make rs1057517358(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108252815

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs1057517358
dbSNP (classic)	rs1057517358
ClinGen	rs1057517358
ebi	rs1057517358
HLI	rs1057517358
Exac	rs1057517358
Gnomad	rs1057517358
Varsome	rs1057517358
LitVar	rs1057517358
Map	rs1057517358
PheGenI	rs1057517358
Biobank	rs1057517358
1000 genomes	rs1057517358
hgdp	rs1057517358
ensembl	rs1057517358
geneview	rs1057517358
scholar	rs1057517358
google	rs1057517358
pharmgkb	rs1057517358
gwascentral	rs1057517358
openSNP	rs1057517358
23andMe	rs1057517358
SNPshot	rs1057517358
SNPdbe	rs1057517358
MSV3d	rs1057517358
GWAS Ctlg	rs1057517358

Max Magnitude

0

ClinVar
Risk	rs1057517358(G;G)
Alt	rs1057517358(G;G)
Reference	Rs1057517358(A;A)
Significance	Probable-Pathogenic
Disease	Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108123542A>G
CLNSRC
CLNACC	RCV000411840.1,