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rs863224440

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224440(A;C)
Make rs863224440(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108332899
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs863224440
ebirs863224440
HLIrs863224440
Exacrs863224440
Varsomers863224440
Maprs863224440
PheGenIrs863224440
hapmaprs863224440
1000 genomesrs863224440
hgdprs863224440
ensemblrs863224440
gopubmedrs863224440
geneviewrs863224440
scholarrs863224440
googlers863224440
pharmgkbrs863224440
gwascentralrs863224440
openSNPrs863224440
23andMers863224440
23andMe allrs863224440
SNP Nexus

SNPshotrs863224440
SNPdbers863224440
MSV3drs863224440
GWAS Ctlgrs863224440
Max Magnitude0
ClinVar
Risk rs863224440(C;C)
Alt rs863224440(C;C)
Reference rs863224440(A;A)
Significance Probable-Pathogenic
Disease Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene C11orf65 ATM
CLNDBN Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108203626A>C
CLNSRC
CLNACC RCV000197870.1, RCV000215938.1,