Have questions? Visit https://www.reddit.com/r/SNPedia

rs876658804

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658804(G;T)
Make rs876658804(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108267201
GeneATM
is asnp
is mentioned by
dbSNPrs876658804
ebirs876658804
HLIrs876658804
Exacrs876658804
Varsomers876658804
Maprs876658804
PheGenIrs876658804
hapmaprs876658804
1000 genomesrs876658804
hgdprs876658804
ensemblrs876658804
gopubmedrs876658804
geneviewrs876658804
scholarrs876658804
googlers876658804
pharmgkbrs876658804
gwascentralrs876658804
openSNPrs876658804
23andMers876658804
23andMe allrs876658804
SNP Nexus

SNPshotrs876658804
SNPdbers876658804
MSV3drs876658804
GWAS Ctlgrs876658804
Max Magnitude0
ClinVar
Risk rs876658804(T;T)
Alt rs876658804(T;T)
Reference rs876658804(G;G)
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.108137928G>T
CLNSRC
CLNACC RCV000218015.1,