rs201089102

Orientation

plus

Stabilized

plus

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

Make rs201089102(G;T)

Make rs201089102(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

108247128

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs201089102
dbSNP (classic)	rs201089102
ClinGen	rs201089102
ebi	rs201089102
HLI	rs201089102
Exac	rs201089102
Gnomad	rs201089102
Varsome	rs201089102
LitVar	rs201089102
Map	rs201089102
PheGenI	rs201089102
Biobank	rs201089102
1000 genomes	rs201089102
hgdp	rs201089102
ensembl	rs201089102
geneview	rs201089102
scholar	rs201089102
google	rs201089102
pharmgkb	rs201089102
gwascentral	rs201089102
openSNP	rs201089102
23andMe	rs201089102
SNPshot	rs201089102
SNPdbe	rs201089102
MSV3d	rs201089102
GWAS Ctlg	rs201089102

Max Magnitude

0

ClinVar
Risk	rs201089102(T;T)
Alt	rs201089102(T;T)
Reference	Rs201089102(G;G)
Significance	Pathogenic
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.108117855G>T
CLNSRC
CLNACC	RCV000166070.3, RCV000411731.1, RCV000436210.1,