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rs876658587

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658587(G;T)
Make rs876658587(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108293475
GeneATM
is asnp
is mentioned by
dbSNPrs876658587
ebirs876658587
HLIrs876658587
Exacrs876658587
Varsomers876658587
Maprs876658587
PheGenIrs876658587
hapmaprs876658587
1000 genomesrs876658587
hgdprs876658587
ensemblrs876658587
gopubmedrs876658587
geneviewrs876658587
scholarrs876658587
googlers876658587
pharmgkbrs876658587
gwascentralrs876658587
openSNPrs876658587
23andMers876658587
23andMe allrs876658587
SNP Nexus

SNPshotrs876658587
SNPdbers876658587
MSV3drs876658587
GWAS Ctlgrs876658587
Max Magnitude0
ClinVar
Risk rs876658587(T;T)
Alt rs876658587(T;T)
Reference rs876658587(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.108164202G>T
CLNSRC
CLNACC RCV000219771.1,