rs876659710

Orientation

plus

Stabilized

plus

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

Make rs876659710(C;C)

Make rs876659710(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108257480

Gene

ATM

is a	snp
is	mentioned by
dbSNP	rs876659710
dbSNP (classic)	rs876659710
ClinGen	rs876659710
ebi	rs876659710
HLI	rs876659710
Exac	rs876659710
Gnomad	rs876659710
Varsome	rs876659710
LitVar	rs876659710
Map	rs876659710
PheGenI	rs876659710
Biobank	rs876659710
1000 genomes	rs876659710
hgdp	rs876659710
ensembl	rs876659710
geneview	rs876659710
scholar	rs876659710
google	rs876659710
pharmgkb	rs876659710
gwascentral	rs876659710
openSNP	rs876659710
23andMe	rs876659710
SNPshot	rs876659710
SNPdbe	rs876659710
MSV3d	rs876659710
GWAS Ctlg	rs876659710

Max Magnitude

0

ClinVar
Risk	rs876659710(C;C)
Alt	rs876659710(C;C)
Reference	Rs876659710(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation	info
Gene	ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108128207G>C
CLNSRC
CLNACC	RCV000223310.1, RCV000464660.1,