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rs778031266

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs778031266(A;A)
Make rs778031266(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108316114
GeneATM
is asnp
is mentioned by
dbSNPrs778031266
ebirs778031266
HLIrs778031266
Exacrs778031266
Varsomers778031266
Maprs778031266
PheGenIrs778031266
hapmaprs778031266
1000 genomesrs778031266
hgdprs778031266
ensemblrs778031266
gopubmedrs778031266
geneviewrs778031266
scholarrs778031266
googlers778031266
pharmgkbrs778031266
gwascentralrs778031266
openSNPrs778031266
23andMers778031266
23andMe allrs778031266
SNP Nexus

SNPshotrs778031266
SNPdbers778031266
MSV3drs778031266
GWAS Ctlgrs778031266
Max Magnitude0
ClinVar
Risk rs778031266(A;A)
Alt rs778031266(A;A)
Reference rs778031266(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108186841G>A
CLNSRC
CLNACC RCV000222023.1,