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rs772821016

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs772821016(C;T)
Make rs772821016(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position108244873
GeneATM
is asnp
is mentioned by
dbSNPrs772821016
ebirs772821016
HLIrs772821016
Exacrs772821016
Varsomers772821016
Maprs772821016
PheGenIrs772821016
hapmaprs772821016
1000 genomesrs772821016
hgdprs772821016
ensemblrs772821016
gopubmedrs772821016
geneviewrs772821016
scholarrs772821016
googlers772821016
pharmgkbrs772821016
gwascentralrs772821016
openSNPrs772821016
23andMers772821016
23andMe allrs772821016
SNP Nexus

SNPshotrs772821016
SNPdbers772821016
MSV3drs772821016
GWAS Ctlgrs772821016
Max Magnitude0
ClinVar
Risk rs772821016(T;T)
Alt rs772821016(T;T)
Reference rs772821016(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene ATM
CLNDBN Ataxia-telangiectasia syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108115600C>T
CLNSRC
CLNACC RCV000196975.1, RCV000216766.1,