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

rs876659283

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659283(G;T)
Make rs876659283(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108251997
GeneATM
is asnp
is mentioned by
dbSNPrs876659283
ebirs876659283
HLIrs876659283
Exacrs876659283
Varsomers876659283
Maprs876659283
PheGenIrs876659283
hapmaprs876659283
1000 genomesrs876659283
hgdprs876659283
ensemblrs876659283
gopubmedrs876659283
geneviewrs876659283
scholarrs876659283
googlers876659283
pharmgkbrs876659283
gwascentralrs876659283
openSNPrs876659283
23andMers876659283
23andMe allrs876659283
SNP Nexus

SNPshotrs876659283
SNPdbers876659283
MSV3drs876659283
GWAS Ctlgrs876659283
Max Magnitude0
ClinVar
Risk rs876659283(T;T)
Alt rs876659283(T;T)
Reference rs876659283(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.108122724G>T
CLNSRC
CLNACC RCV000220061.1,