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rs730881299

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881299(-;-)
Make rs730881299(-;T)
Make rs730881299(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108267268
GeneATM
is asnp
is mentioned by
dbSNPrs730881299
ebirs730881299
HLIrs730881299
Exacrs730881299
Varsomers730881299
Maprs730881299
PheGenIrs730881299
hapmaprs730881299
1000 genomesrs730881299
hgdprs730881299
ensemblrs730881299
gopubmedrs730881299
geneviewrs730881299
scholarrs730881299
googlers730881299
pharmgkbrs730881299
gwascentralrs730881299
openSNPrs730881299
23andMers730881299
23andMe allrs730881299
SNP Nexus

SNPshotrs730881299
SNPdbers730881299
MSV3drs730881299
GWAS Ctlgrs730881299
Max Magnitude0
ClinVar
Risk rs730881299(T;T)
Alt rs730881299(T;T)
Reference rs730881299(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000011.9:g.108137995dupT
CLNSRC
CLNACC RCV000159628.1,