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rs730881304

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881304(-;-)
Make rs730881304(-;T)
Make rs730881304(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108293326
GeneATM
is asnp
is mentioned by
dbSNPrs730881304
ebirs730881304
HLIrs730881304
Exacrs730881304
Varsomers730881304
Maprs730881304
PheGenIrs730881304
hapmaprs730881304
1000 genomesrs730881304
hgdprs730881304
ensemblrs730881304
gopubmedrs730881304
geneviewrs730881304
scholarrs730881304
googlers730881304
pharmgkbrs730881304
gwascentralrs730881304
openSNPrs730881304
23andMers730881304
23andMe allrs730881304
SNP Nexus

SNPshotrs730881304
SNPdbers730881304
MSV3drs730881304
GWAS Ctlgrs730881304
Max Magnitude0
ClinVar
Risk rs730881304(T;T)
Alt rs730881304(T;T)
Reference rs730881304(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108164053dupT
CLNSRC
CLNACC RCV000159633.1,