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rs876658899

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658899(-;-)
Make rs876658899(-;A)
Make rs876658899(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108281102
GeneATM
is asnp
is mentioned by
dbSNPrs876658899
ebirs876658899
HLIrs876658899
Exacrs876658899
Varsomers876658899
Maprs876658899
PheGenIrs876658899
hapmaprs876658899
1000 genomesrs876658899
hgdprs876658899
ensemblrs876658899
gopubmedrs876658899
geneviewrs876658899
scholarrs876658899
googlers876658899
pharmgkbrs876658899
gwascentralrs876658899
openSNPrs876658899
23andMers876658899
23andMe allrs876658899
SNP Nexus

SNPshotrs876658899
SNPdbers876658899
MSV3drs876658899
GWAS Ctlgrs876658899
Max Magnitude0
ClinVar
Risk rs876658899(A;A)
Alt rs876658899(A;A)
Reference rs876658899(;)
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.108151829dupA
CLNSRC
CLNACC RCV000222552.1,