rs587779865

Orientation

plus

Stabilized

plus

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

Make rs587779865(C;T)

Make rs587779865(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108330362

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587779865
dbSNP (classic)	rs587779865
ClinGen	rs587779865
ebi	rs587779865
HLI	rs587779865
Exac	rs587779865
Gnomad	rs587779865
Varsome	rs587779865
LitVar	rs587779865
Map	rs587779865
PheGenI	rs587779865
Biobank	rs587779865
1000 genomes	rs587779865
hgdp	rs587779865
ensembl	rs587779865
geneview	rs587779865
scholar	rs587779865
google	rs587779865
pharmgkb	rs587779865
gwascentral	rs587779865
openSNP	rs587779865
23andMe	rs587779865
SNPshot	rs587779865
SNPdbe	rs587779865
MSV3d	rs587779865
GWAS Ctlg	rs587779865

Max Magnitude

0

ClinVar
Risk	rs587779865(T;T)
Alt	rs587779865(T;T)
Reference	Rs587779865(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Ataxia-telangiectasia syndrome
Variation	info
Gene	C11orf65 ATM
CLNDBN	Hereditary cancer-predisposing syndrome not provided Ataxia-telangiectasia syndrome
Reversed	0
HGVS	NC_000011.9:g.108201089C>T
CLNSRC
CLNACC	RCV000115251.5, RCV000212068.1, RCV000462583.1,