rs1057516590

Orientation

plus

Stabilized

plus

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

Make rs1057516590(-;-)

Make rs1057516590(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108271397

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs1057516590
dbSNP (classic)	rs1057516590
ClinGen	rs1057516590
ebi	rs1057516590
HLI	rs1057516590
Exac	rs1057516590
Gnomad	rs1057516590
Varsome	rs1057516590
LitVar	rs1057516590
Map	rs1057516590
PheGenI	rs1057516590
Biobank	rs1057516590
1000 genomes	rs1057516590
hgdp	rs1057516590
ensembl	rs1057516590
geneview	rs1057516590
scholar	rs1057516590
google	rs1057516590
pharmgkb	rs1057516590
gwascentral	rs1057516590
openSNP	rs1057516590
23andMe	rs1057516590
SNPshot	rs1057516590
SNPdbe	rs1057516590
MSV3d	rs1057516590
GWAS Ctlg	rs1057516590

Max Magnitude

0

ClinVar
Risk	rs1057516590(-;-)
Alt	rs1057516590(-;-)
Reference	Rs1057516590(G;G)
Significance	Probable-Pathogenic
Disease	Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108142124delG
CLNSRC
CLNACC	RCV000411095.1,