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rs587779846

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779846(-;-)
Make rs587779846(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108301760
GeneATM
is asnp
is mentioned by
dbSNPrs587779846
ebirs587779846
HLIrs587779846
Exacrs587779846
Varsomers587779846
Maprs587779846
PheGenIrs587779846
hapmaprs587779846
1000 genomesrs587779846
hgdprs587779846
ensemblrs587779846
gopubmedrs587779846
geneviewrs587779846
scholarrs587779846
googlers587779846
pharmgkbrs587779846
gwascentralrs587779846
openSNPrs587779846
23andMers587779846
23andMe allrs587779846
SNP Nexus

SNPshotrs587779846
SNPdbers587779846
MSV3drs587779846
GWAS Ctlgrs587779846
Max Magnitude0
ClinVar
Risk rs587779846(;)
Alt rs587779846(;)
Reference rs587779846(C;C)
Significance Other
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108172487delC
CLNSRC
CLNACC RCV000115210.5, RCV000169483.2, RCV000235105.1,