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rs730881310

From SNPedia

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Geno Mag Summary
(TCTA;TCTA) 0 common in clinvar
Make rs730881310(-;-)
Make rs730881310(-;TCTA)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position108302848
GeneATM
is asnp
is mentioned by
dbSNPrs730881310
ebirs730881310
HLIrs730881310
Exacrs730881310
Varsomers730881310
Maprs730881310
PheGenIrs730881310
hapmaprs730881310
1000 genomesrs730881310
hgdprs730881310
ensemblrs730881310
gopubmedrs730881310
geneviewrs730881310
scholarrs730881310
googlers730881310
pharmgkbrs730881310
gwascentralrs730881310
openSNPrs730881310
23andMers730881310
23andMe allrs730881310
SNP Nexus

SNPshotrs730881310
SNPdbers730881310
MSV3drs730881310
GWAS Ctlgrs730881310
Max Magnitude0
ClinVar
Risk rs730881310(;)
Alt rs730881310(;)
Reference rs730881310(TCTA;TCTA)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome
Variation info
Gene ATM
CLNDBN Hereditary cancer-predisposing syndrome Tumor susceptibility linked to germline BAP1 mutations Ataxia-telangiectasia syndrome
Reversed 0
HGVS NC_000011.9:g.108173575_108173578delTCTA
CLNSRC
CLNACC RCV000159640.1, RCV000217813.1, RCV000232019.1,