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rs587781967

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781967(C;T)
Make rs587781967(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108335878
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587781967
ebirs587781967
HLIrs587781967
Exacrs587781967
Varsomers587781967
Maprs587781967
PheGenIrs587781967
hapmaprs587781967
1000 genomesrs587781967
hgdprs587781967
ensemblrs587781967
gopubmedrs587781967
geneviewrs587781967
scholarrs587781967
googlers587781967
pharmgkbrs587781967
gwascentralrs587781967
openSNPrs587781967
23andMers587781967
23andMe allrs587781967
SNP Nexus

SNPshotrs587781967
SNPdbers587781967
MSV3drs587781967
GWAS Ctlgrs587781967
Max Magnitude0
ClinVar
Risk rs587781967(T;T)
Alt rs587781967(T;T)
Reference rs587781967(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.108206605C>T
CLNSRC
CLNACC RCV000130347.2,