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rs876660315

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660315(-;-)
Make rs876660315(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108244098
GeneATM
is asnp
is mentioned by
dbSNPrs876660315
ebirs876660315
HLIrs876660315
Exacrs876660315
Varsomers876660315
Maprs876660315
PheGenIrs876660315
hapmaprs876660315
1000 genomesrs876660315
hgdprs876660315
ensemblrs876660315
gopubmedrs876660315
geneviewrs876660315
scholarrs876660315
googlers876660315
pharmgkbrs876660315
gwascentralrs876660315
openSNPrs876660315
23andMers876660315
23andMe allrs876660315
SNP Nexus

SNPshotrs876660315
SNPdbers876660315
MSV3drs876660315
GWAS Ctlgrs876660315
Max Magnitude0
ClinVar
Risk rs876660315(;)
Alt rs876660315(;)
Reference rs876660315(C;C)
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.108114825delC
CLNSRC
CLNACC RCV000219456.1,