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rs587779851

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779851(CCT;CCT)
Make rs587779851(CCT;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108310188
GeneATM
is asnp
is mentioned by
dbSNPrs587779851
ebirs587779851
HLIrs587779851
Exacrs587779851
Varsomers587779851
Maprs587779851
PheGenIrs587779851
hapmaprs587779851
1000 genomesrs587779851
hgdprs587779851
ensemblrs587779851
gopubmedrs587779851
geneviewrs587779851
scholarrs587779851
googlers587779851
pharmgkbrs587779851
gwascentralrs587779851
openSNPrs587779851
23andMers587779851
23andMe allrs587779851
SNP Nexus

SNPshotrs587779851
SNPdbers587779851
MSV3drs587779851
GWAS Ctlgrs587779851
Max Magnitude0
ClinVar
Risk rs587779851(CCT;CCT)
Alt rs587779851(CCT;CCT)
Reference rs587779851(G;G)
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.108180915delGinsCCT
CLNSRC
CLNACC RCV000115216.5, RCV000235106.1,