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rs876659454

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659454(C;T)
Make rs876659454(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108315898
GeneATM
is asnp
is mentioned by
dbSNPrs876659454
ebirs876659454
HLIrs876659454
Exacrs876659454
Varsomers876659454
Maprs876659454
PheGenIrs876659454
hapmaprs876659454
1000 genomesrs876659454
hgdprs876659454
ensemblrs876659454
gopubmedrs876659454
geneviewrs876659454
scholarrs876659454
googlers876659454
pharmgkbrs876659454
gwascentralrs876659454
openSNPrs876659454
23andMers876659454
23andMe allrs876659454
SNP Nexus

SNPshotrs876659454
SNPdbers876659454
MSV3drs876659454
GWAS Ctlgrs876659454
Max Magnitude0
ClinVar
Risk rs876659454(T;T)
Alt rs876659454(T;T)
Reference rs876659454(C;C)
Significance 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.108186625C>T
CLNSRC
CLNACC RCV000213485.1,