Have questions? Visit https://www.reddit.com/r/SNPedia

rs587781963

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781963(C;T)
Make rs587781963(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108310255
GeneATM
is asnp
is mentioned by
dbSNPrs587781963
ebirs587781963
HLIrs587781963
Exacrs587781963
Varsomers587781963
Maprs587781963
PheGenIrs587781963
hapmaprs587781963
1000 genomesrs587781963
hgdprs587781963
ensemblrs587781963
gopubmedrs587781963
geneviewrs587781963
scholarrs587781963
googlers587781963
pharmgkbrs587781963
gwascentralrs587781963
openSNPrs587781963
23andMers587781963
23andMe allrs587781963
SNP Nexus

SNPshotrs587781963
SNPdbers587781963
MSV3drs587781963
GWAS Ctlgrs587781963
Max Magnitude0
ClinVar
Risk rs587781963(T;T)
Alt rs587781963(T;T)
Reference rs587781963(C;C)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108180982C>T
CLNSRC
CLNACC RCV000130342.2,