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

rs587779836

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779836(A;A)
Make rs587779836(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108284316
GeneATM
is asnp
is mentioned by
dbSNPrs587779836
ebirs587779836
HLIrs587779836
Exacrs587779836
Varsomers587779836
Maprs587779836
PheGenIrs587779836
hapmaprs587779836
1000 genomesrs587779836
hgdprs587779836
ensemblrs587779836
gopubmedrs587779836
geneviewrs587779836
scholarrs587779836
googlers587779836
pharmgkbrs587779836
gwascentralrs587779836
openSNPrs587779836
23andMers587779836
23andMe allrs587779836
SNP Nexus

SNPshotrs587779836
SNPdbers587779836
MSV3drs587779836
GWAS Ctlgrs587779836
Max Magnitude0
ClinVar
Risk rs587779836(A;A)
Alt rs587779836(A;A)
Reference rs587779836(G;G)
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.108155043G>A
CLNSRC
CLNACC RCV000115181.5, RCV000212003.1,