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rs587781353

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587781353(AA;AA)
Make rs587781353(AA;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108345889
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587781353
ebirs587781353
HLIrs587781353
Exacrs587781353
Varsomers587781353
Maprs587781353
PheGenIrs587781353
hapmaprs587781353
1000 genomesrs587781353
hgdprs587781353
ensemblrs587781353
gopubmedrs587781353
geneviewrs587781353
scholarrs587781353
googlers587781353
pharmgkbrs587781353
gwascentralrs587781353
openSNPrs587781353
23andMers587781353
23andMe allrs587781353
SNP Nexus

SNPshotrs587781353
SNPdbers587781353
MSV3drs587781353
GWAS Ctlgrs587781353
Max Magnitude0
Mentioned as a pathogenic/likely pathogenic mutation associated with cancer predisposition in [PMID 26681312OA-icon.png]
ClinVar
Risk rs587781353(AA;AA)
Alt rs587781353(AA;AA)
Reference rs587781353(TG;TG)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108216616_108216617delTGinsAA
CLNSRC
CLNACC RCV000129137.5, RCV000235111.1,