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rs587779869

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779869(-;-)
Make rs587779869(-;T)
Make rs587779869(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108333956
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs587779869
ebirs587779869
HLIrs587779869
Exacrs587779869
Varsomers587779869
Maprs587779869
PheGenIrs587779869
hapmaprs587779869
1000 genomesrs587779869
hgdprs587779869
ensemblrs587779869
gopubmedrs587779869
geneviewrs587779869
scholarrs587779869
googlers587779869
pharmgkbrs587779869
gwascentralrs587779869
openSNPrs587779869
23andMers587779869
23andMe allrs587779869
SNP Nexus

SNPshotrs587779869
SNPdbers587779869
MSV3drs587779869
GWAS Ctlgrs587779869
Max Magnitude0
ClinVar
Risk rs587779869(T;T)
Alt rs587779869(T;T)
Reference rs587779869(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108204683dupT
CLNSRC
CLNACC RCV000115259.4,