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rs876660780

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660780(C;G)
Make rs876660780(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108268443
GeneATM
is asnp
is mentioned by
dbSNPrs876660780
ebirs876660780
HLIrs876660780
Exacrs876660780
Varsomers876660780
Maprs876660780
PheGenIrs876660780
hapmaprs876660780
1000 genomesrs876660780
hgdprs876660780
ensemblrs876660780
gopubmedrs876660780
geneviewrs876660780
scholarrs876660780
googlers876660780
pharmgkbrs876660780
gwascentralrs876660780
openSNPrs876660780
23andMers876660780
23andMe allrs876660780
SNP Nexus

SNPshotrs876660780
SNPdbers876660780
MSV3drs876660780
GWAS Ctlgrs876660780
Max Magnitude0
ClinVar
Risk rs876660780(G;G)
Alt rs876660780(G;G)
Reference rs876660780(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.108139170C>G
CLNSRC
CLNACC RCV000218040.1,