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rs876658287

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658287(-;-)
Make rs876658287(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108304727
GeneATM
is asnp
is mentioned by
dbSNPrs876658287
ebirs876658287
HLIrs876658287
Exacrs876658287
Varsomers876658287
Maprs876658287
PheGenIrs876658287
hapmaprs876658287
1000 genomesrs876658287
hgdprs876658287
ensemblrs876658287
gopubmedrs876658287
geneviewrs876658287
scholarrs876658287
googlers876658287
pharmgkbrs876658287
gwascentralrs876658287
openSNPrs876658287
23andMers876658287
23andMe allrs876658287
SNP Nexus

SNPshotrs876658287
SNPdbers876658287
MSV3drs876658287
GWAS Ctlgrs876658287
Max Magnitude0
ClinVar
Risk rs876658287(;)
Alt rs876658287(;)
Reference rs876658287(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000011.9:g.108175454delT
CLNSRC
CLNACC RCV000219889.1, RCV000236989.1,