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rs587781837

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781837(-;-)
Make rs587781837(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108343350
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587781837
ebirs587781837
HLIrs587781837
Exacrs587781837
Varsomers587781837
Maprs587781837
PheGenIrs587781837
hapmaprs587781837
1000 genomesrs587781837
hgdprs587781837
ensemblrs587781837
gopubmedrs587781837
geneviewrs587781837
scholarrs587781837
googlers587781837
pharmgkbrs587781837
gwascentralrs587781837
openSNPrs587781837
23andMers587781837
23andMe allrs587781837
SNP Nexus

SNPshotrs587781837
SNPdbers587781837
MSV3drs587781837
GWAS Ctlgrs587781837
Max Magnitude0
ClinVar
Risk rs587781837(;)
Alt rs587781837(;)
Reference rs587781837(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108214077delT
CLNSRC
CLNACC RCV000130132.2,