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rs139770721

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139770721(A;A)
Make rs139770721(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108315911
GeneATM
is asnp
is mentioned by
dbSNPrs139770721
ebirs139770721
HLIrs139770721
Exacrs139770721
Varsomers139770721
Maprs139770721
PheGenIrs139770721
hapmaprs139770721
1000 genomesrs139770721
hgdprs139770721
ensemblrs139770721
gopubmedrs139770721
geneviewrs139770721
scholarrs139770721
googlers139770721
pharmgkbrs139770721
gwascentralrs139770721
openSNPrs139770721
23andMers139770721
23andMe allrs139770721
SNP Nexus

SNPshotrs139770721
SNPdbers139770721
MSV3drs139770721
GWAS Ctlgrs139770721
Max Magnitude0
ClinVar
Risk rs139770721(A;A)
Alt rs139770721(A;A)
Reference rs139770721(G;G)
Significance Other
Disease Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided
Reversed 0
HGVS NC_000011.9:g.108186638G>A
CLNSRC
CLNACC RCV000159742.3, RCV000167946.3, RCV000212037.1,