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

rs587781302

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587781302(A;G)
Make rs587781302(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108315863
GeneATM
is asnp
is mentioned by
dbSNPrs587781302
ebirs587781302
HLIrs587781302
Exacrs587781302
Varsomers587781302
Maprs587781302
PheGenIrs587781302
hapmaprs587781302
1000 genomesrs587781302
hgdprs587781302
ensemblrs587781302
gopubmedrs587781302
geneviewrs587781302
scholarrs587781302
googlers587781302
pharmgkbrs587781302
gwascentralrs587781302
openSNPrs587781302
23andMers587781302
23andMe allrs587781302
SNP Nexus

SNPshotrs587781302
SNPdbers587781302
MSV3drs587781302
GWAS Ctlgrs587781302
Max Magnitude0
ClinVar
Risk rs587781302(G;G)
Alt rs587781302(G;G)
Reference rs587781302(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108186590A>G
CLNSRC
CLNACC RCV000129013.2,