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rs730881336

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730881336(C;T)
Make rs730881336(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108244867
GeneATM
is asnp
is mentioned by
dbSNPrs730881336
ebirs730881336
HLIrs730881336
Exacrs730881336
Varsomers730881336
Maprs730881336
PheGenIrs730881336
hapmaprs730881336
1000 genomesrs730881336
hgdprs730881336
ensemblrs730881336
gopubmedrs730881336
geneviewrs730881336
scholarrs730881336
googlers730881336
pharmgkbrs730881336
gwascentralrs730881336
openSNPrs730881336
23andMers730881336
23andMe allrs730881336
SNP Nexus

SNPshotrs730881336
SNPdbers730881336
MSV3drs730881336
GWAS Ctlgrs730881336
Max Magnitude0
ClinVar
Risk rs730881336(T;T)
Alt rs730881336(T;T)
Reference rs730881336(C;C)
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.108115594C>T
CLNSRC
CLNACC RCV000159678.3, RCV000211945.1,