rs876660382

Orientation

plus

Stabilized

plus

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

Make rs876660382(G;T)

Make rs876660382(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

108365356

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs876660382
dbSNP (classic)	rs876660382
ClinGen	rs876660382
ebi	rs876660382
HLI	rs876660382
Exac	rs876660382
Gnomad	rs876660382
Varsome	rs876660382
LitVar	rs876660382
Map	rs876660382
PheGenI	rs876660382
Biobank	rs876660382
1000 genomes	rs876660382
hgdp	rs876660382
ensembl	rs876660382
geneview	rs876660382
scholar	rs876660382
google	rs876660382
pharmgkb	rs876660382
gwascentral	rs876660382
openSNP	rs876660382
23andMe	rs876660382
SNPshot	rs876660382
SNPdbe	rs876660382
MSV3d	rs876660382
GWAS Ctlg	rs876660382

Max Magnitude

0

ClinVar
Risk	rs876660382(T;T)
Alt	rs876660382(T;T)
Reference	Rs876660382(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed	0
HGVS	NC_000011.9:g.108236083G>T
CLNSRC
CLNACC	RCV000222768.2, RCV000233073.1, RCV000255661.1,