Have questions? Visit https://www.reddit.com/r/SNPedia

rs587781831

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781831(-;-)
Make rs587781831(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108235719
GeneATM
is asnp
is mentioned by
dbSNPrs587781831
ebirs587781831
HLIrs587781831
Exacrs587781831
Varsomers587781831
Maprs587781831
PheGenIrs587781831
hapmaprs587781831
1000 genomesrs587781831
hgdprs587781831
ensemblrs587781831
gopubmedrs587781831
geneviewrs587781831
scholarrs587781831
googlers587781831
pharmgkbrs587781831
gwascentralrs587781831
openSNPrs587781831
23andMers587781831
23andMe allrs587781831
SNP Nexus

SNPshotrs587781831
SNPdbers587781831
MSV3drs587781831
GWAS Ctlgrs587781831
Max Magnitude0
ClinVar
Risk rs587781831(;)
Alt rs587781831(;)
Reference rs587781831(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108106446delA
CLNSRC
CLNACC RCV000130118.2,