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rs587781598

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs587781598(-;-)
Make rs587781598(-;TG)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108250755
GeneATM
is asnp
is mentioned by
dbSNPrs587781598
ebirs587781598
HLIrs587781598
Exacrs587781598
Varsomers587781598
Maprs587781598
PheGenIrs587781598
hapmaprs587781598
1000 genomesrs587781598
hgdprs587781598
ensemblrs587781598
gopubmedrs587781598
geneviewrs587781598
scholarrs587781598
googlers587781598
pharmgkbrs587781598
gwascentralrs587781598
openSNPrs587781598
23andMers587781598
23andMe allrs587781598
SNP Nexus

SNPshotrs587781598
SNPdbers587781598
MSV3drs587781598
GWAS Ctlgrs587781598
Max Magnitude0
ClinVar
Risk rs587781598(;)
Alt rs587781598(;)
Reference rs587781598(TG;TG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108121482_108121483delTG
CLNSRC
CLNACC RCV000129663.2, RCV000236686.1,