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rs587781653

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587781653(-;-)
Make rs587781653(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108289738
GeneATM
is asnp
is mentioned by
dbSNPrs587781653
ebirs587781653
HLIrs587781653
Exacrs587781653
Varsomers587781653
Maprs587781653
PheGenIrs587781653
hapmaprs587781653
1000 genomesrs587781653
hgdprs587781653
ensemblrs587781653
gopubmedrs587781653
geneviewrs587781653
scholarrs587781653
googlers587781653
pharmgkbrs587781653
gwascentralrs587781653
openSNPrs587781653
23andMers587781653
23andMe allrs587781653
SNP Nexus

SNPshotrs587781653
SNPdbers587781653
MSV3drs587781653
GWAS Ctlgrs587781653
Max Magnitude0
ClinVar
Risk rs587781653(;)
Alt rs587781653(;)
Reference rs587781653(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108160465delG
CLNSRC
CLNACC RCV000129787.3,