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rs730881326

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730881326(C;C)
Make rs730881326(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108345910
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs730881326
ebirs730881326
HLIrs730881326
Exacrs730881326
Varsomers730881326
Maprs730881326
PheGenIrs730881326
hapmaprs730881326
1000 genomesrs730881326
hgdprs730881326
ensemblrs730881326
gopubmedrs730881326
geneviewrs730881326
scholarrs730881326
googlers730881326
pharmgkbrs730881326
gwascentralrs730881326
openSNPrs730881326
23andMers730881326
23andMe allrs730881326
SNP Nexus

SNPshotrs730881326
SNPdbers730881326
MSV3drs730881326
GWAS Ctlgrs730881326
Max Magnitude0
ClinVar
Risk rs730881326(C;C)
Alt rs730881326(C;C)
Reference rs730881326(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene C11orf65 ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108216637T>C
CLNSRC
CLNACC RCV000159662.1,