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rs587781698

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781698(C;T)
Make rs587781698(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108365335
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587781698
ebirs587781698
HLIrs587781698
Exacrs587781698
Varsomers587781698
Maprs587781698
PheGenIrs587781698
hapmaprs587781698
1000 genomesrs587781698
hgdprs587781698
ensemblrs587781698
gopubmedrs587781698
geneviewrs587781698
scholarrs587781698
googlers587781698
pharmgkbrs587781698
gwascentralrs587781698
openSNPrs587781698
23andMers587781698
23andMe allrs587781698
SNP Nexus

SNPshotrs587781698
SNPdbers587781698
MSV3drs587781698
GWAS Ctlgrs587781698
Max Magnitude0
ClinVar
Risk rs587781698(T;T)
Alt rs587781698(T;T)
Reference rs587781698(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.108236062C>T
CLNSRC
CLNACC RCV000129865.2,