rs876660567

Orientation

plus

Stabilized

plus

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

Make rs876660567(-;-)

Make rs876660567(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108354826

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876660567
dbSNP (classic)	rs876660567
ClinGen	rs876660567
ebi	rs876660567
HLI	rs876660567
Exac	rs876660567
Gnomad	rs876660567
Varsome	rs876660567
LitVar	rs876660567
Map	rs876660567
PheGenI	rs876660567
Biobank	rs876660567
1000 genomes	rs876660567
hgdp	rs876660567
ensembl	rs876660567
geneview	rs876660567
scholar	rs876660567
google	rs876660567
pharmgkb	rs876660567
gwascentral	rs876660567
openSNP	rs876660567
23andMe	rs876660567
SNPshot	rs876660567
SNPdbe	rs876660567
MSV3d	rs876660567
GWAS Ctlg	rs876660567

Max Magnitude

0

ClinVar
Risk	rs876660567(-;-)
Alt	rs876660567(-;-)
Reference	Rs876660567(C;C)
Significance	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.108225553delC
CLNSRC
CLNACC	RCV000218511.1, RCV000410819.1,