rs876658502

Orientation

plus

Stabilized

plus

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

Make rs876658502(-;A)

Make rs876658502(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108272539

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876658502
dbSNP (classic)	rs876658502
ClinGen	rs876658502
ebi	rs876658502
HLI	rs876658502
Exac	rs876658502
Gnomad	rs876658502
Varsome	rs876658502
LitVar	rs876658502
Map	rs876658502
PheGenI	rs876658502
Biobank	rs876658502
1000 genomes	rs876658502
hgdp	rs876658502
ensembl	rs876658502
geneview	rs876658502
scholar	rs876658502
google	rs876658502
pharmgkb	rs876658502
gwascentral	rs876658502
openSNP	rs876658502
23andMe	rs876658502
SNPshot	rs876658502
SNPdbe	rs876658502
MSV3d	rs876658502
GWAS Ctlg	rs876658502

Max Magnitude

0

ClinVar
Risk	rs876658502(A;A)
Alt	rs876658502(A;A)
Reference	Rs876658502(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome not provided Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108143266dupA
CLNSRC
CLNACC	RCV000220687.1, RCV000236766.1, RCV000462008.1,