rs876659350

Orientation

plus

Stabilized

plus

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

Make rs876659350(-;-)

Make rs876659350(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108333969

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876659350
dbSNP (classic)	rs876659350
ClinGen	rs876659350
ebi	rs876659350
HLI	rs876659350
Exac	rs876659350
Gnomad	rs876659350
Varsome	rs876659350
LitVar	rs876659350
Map	rs876659350
PheGenI	rs876659350
Biobank	rs876659350
1000 genomes	rs876659350
hgdp	rs876659350
ensembl	rs876659350
geneview	rs876659350
scholar	rs876659350
google	rs876659350
pharmgkb	rs876659350
gwascentral	rs876659350
openSNP	rs876659350
23andMe	rs876659350
SNPshot	rs876659350
SNPdbe	rs876659350
MSV3d	rs876659350
GWAS Ctlg	rs876659350

Max Magnitude

0

ClinVar
Risk	rs876659350(-;-)
Alt	rs876659350(-;-)
Reference	Rs876659350(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108204696delG
CLNSRC
CLNACC	RCV000213901.1, RCV000475897.1,