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rs587779865

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779865(C;T)
Make rs587779865(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108330362
GeneATM
is asnp
is mentioned by
dbSNPrs587779865
ebirs587779865
HLIrs587779865
Exacrs587779865
Varsomers587779865
Maprs587779865
PheGenIrs587779865
hapmaprs587779865
1000 genomesrs587779865
hgdprs587779865
ensemblrs587779865
gopubmedrs587779865
geneviewrs587779865
scholarrs587779865
googlers587779865
pharmgkbrs587779865
gwascentralrs587779865
openSNPrs587779865
23andMers587779865
23andMe allrs587779865
SNP Nexus

SNPshotrs587779865
SNPdbers587779865
MSV3drs587779865
GWAS Ctlgrs587779865
Max Magnitude0
ClinVar
Risk rs587779865(T;T)
Alt rs587779865(T;T)
Reference rs587779865(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108201089C>T
CLNSRC
CLNACC RCV000115251.4, RCV000212068.1,