rs587781672

Orientation

plus

Stabilized

plus

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

Make rs587781672(G;T)

Make rs587781672(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108329027

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587781672
dbSNP (classic)	rs587781672
ClinGen	rs587781672
ebi	rs587781672
HLI	rs587781672
Exac	rs587781672
Gnomad	rs587781672
Varsome	rs587781672
LitVar	rs587781672
Map	rs587781672
PheGenI	rs587781672
Biobank	rs587781672
1000 genomes	rs587781672
hgdp	rs587781672
ensembl	rs587781672
geneview	rs587781672
scholar	rs587781672
google	rs587781672
pharmgkb	rs587781672
gwascentral	rs587781672
openSNP	rs587781672
23andMe	rs587781672
SNPshot	rs587781672
SNPdbe	rs587781672
MSV3d	rs587781672
GWAS Ctlg	rs587781672

Max Magnitude

0

ClinVar
Risk	rs587781672(T;T)
Alt	rs587781672(T;T)
Reference	Rs587781672(G;G)
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.108199754G>T
CLNSRC
CLNACC	RCV000129830.3, RCV000169152.1,