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rs777849257

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777849257(C;T)
Make rs777849257(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108253938
GeneATM
is asnp
is mentioned by
dbSNPrs777849257
ebirs777849257
HLIrs777849257
Exacrs777849257
Varsomers777849257
Maprs777849257
PheGenIrs777849257
hapmaprs777849257
1000 genomesrs777849257
hgdprs777849257
ensemblrs777849257
gopubmedrs777849257
geneviewrs777849257
scholarrs777849257
googlers777849257
pharmgkbrs777849257
gwascentralrs777849257
openSNPrs777849257
23andMers777849257
23andMe allrs777849257
SNP Nexus

SNPshotrs777849257
SNPdbers777849257
MSV3drs777849257
GWAS Ctlgrs777849257
Max Magnitude0
ClinVar
Risk rs777849257(T;T)
Alt rs777849257(T;T)
Reference rs777849257(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108124665C>T
CLNSRC
CLNACC RCV000215540.1,