rs1057516442

Orientation

plus

Stabilized

plus

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

Make rs1057516442(A;T)

Make rs1057516442(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

108245002

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs1057516442
dbSNP (classic)	rs1057516442
ClinGen	rs1057516442
ebi	rs1057516442
HLI	rs1057516442
Exac	rs1057516442
Gnomad	rs1057516442
Varsome	rs1057516442
LitVar	rs1057516442
Map	rs1057516442
PheGenI	rs1057516442
Biobank	rs1057516442
1000 genomes	rs1057516442
hgdp	rs1057516442
ensembl	rs1057516442
geneview	rs1057516442
scholar	rs1057516442
google	rs1057516442
pharmgkb	rs1057516442
gwascentral	rs1057516442
openSNP	rs1057516442
23andMe	rs1057516442
SNPshot	rs1057516442
SNPdbe	rs1057516442
MSV3d	rs1057516442
GWAS Ctlg	rs1057516442

Max Magnitude

0

ClinVar
Risk	rs1057516442(T;T)
Alt	rs1057516442(T;T)
Reference	Rs1057516442(A;A)
Significance	Probable-Pathogenic
Disease	Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108115729A>T
CLNSRC
CLNACC	RCV000411113.1,