rs587779872

Orientation

plus

Stabilized

plus

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

Make rs587779872(C;T)

Make rs587779872(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

108345818

Gene	ATM, C11orf65

is a	snp
is	mentioned by
dbSNP	rs587779872
dbSNP (classic)	rs587779872
ClinGen	rs587779872
ebi	rs587779872
HLI	rs587779872
Exac	rs587779872
Gnomad	rs587779872
Varsome	rs587779872
LitVar	rs587779872
Map	rs587779872
PheGenI	rs587779872
Biobank	rs587779872
1000 genomes	rs587779872
hgdp	rs587779872
ensembl	rs587779872
geneview	rs587779872
scholar	rs587779872
google	rs587779872
pharmgkb	rs587779872
gwascentral	rs587779872
openSNP	rs587779872
23andMe	rs587779872
SNPshot	rs587779872
SNPdbe	rs587779872
MSV3d	rs587779872
GWAS Ctlg	rs587779872

Max Magnitude

0

ClinVar
Risk	rs587779872(T;T)
Alt	rs587779872(T;T)
Reference	Rs587779872(C;C)
Significance	Other
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.108216545C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000115265.7, RCV000169354.5, RCV000212084.2,