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rs876660485

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660485(C;T)
Make rs876660485(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108250861
GeneATM
is asnp
is mentioned by
dbSNPrs876660485
ebirs876660485
HLIrs876660485
Exacrs876660485
Varsomers876660485
Maprs876660485
PheGenIrs876660485
hapmaprs876660485
1000 genomesrs876660485
hgdprs876660485
ensemblrs876660485
gopubmedrs876660485
geneviewrs876660485
scholarrs876660485
googlers876660485
pharmgkbrs876660485
gwascentralrs876660485
openSNPrs876660485
23andMers876660485
23andMe allrs876660485
SNP Nexus

SNPshotrs876660485
SNPdbers876660485
MSV3drs876660485
GWAS Ctlgrs876660485
Max Magnitude0
ClinVar
Risk rs876660485(T;T)
Alt rs876660485(T;T)
Reference rs876660485(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.108121588C>T
CLNSRC
CLNACC RCV000221369.1,