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rs587781363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781363(C;T)
Make rs587781363(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108345797
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587781363
ClinGenrs587781363
ebirs587781363
HLIrs587781363
Exacrs587781363
Varsomers587781363
Maprs587781363
PheGenIrs587781363
hapmaprs587781363
1000 genomesrs587781363
hgdprs587781363
ensemblrs587781363
gopubmedrs587781363
geneviewrs587781363
scholarrs587781363
googlers587781363
pharmgkbrs587781363
gwascentralrs587781363
openSNPrs587781363
23andMers587781363
23andMe allrs587781363
SNP Nexus

SNPshotrs587781363
SNPdbers587781363
MSV3drs587781363
GWAS Ctlgrs587781363
Max Magnitude0
ClinVar
Risk rs587781363(T;T)
Alt rs587781363(T;T)
Reference Rs587781363(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108216524C>T
CLNSRC
CLNACC RCV000129156.3,