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

rs587779866

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779866(A;C)
Make rs587779866(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108331877
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587779866
ebirs587779866
HLIrs587779866
Exacrs587779866
Varsomers587779866
Maprs587779866
PheGenIrs587779866
hapmaprs587779866
1000 genomesrs587779866
hgdprs587779866
ensemblrs587779866
gopubmedrs587779866
geneviewrs587779866
scholarrs587779866
googlers587779866
pharmgkbrs587779866
gwascentralrs587779866
openSNPrs587779866
23andMers587779866
23andMe allrs587779866
SNP Nexus

SNPshotrs587779866
SNPdbers587779866
MSV3drs587779866
GWAS Ctlgrs587779866
Max Magnitude0
ClinVar
Risk rs587779866(C;C)
Alt rs587779866(C;C)
Reference rs587779866(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108202604A>C
CLNSRC
CLNACC RCV000115253.5, RCV000206201.2, RCV000212074.1,