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rs876659710

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659710(C;C)
Make rs876659710(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108257480
GeneATM
is asnp
is mentioned by
dbSNPrs876659710
ebirs876659710
HLIrs876659710
Exacrs876659710
Varsomers876659710
Maprs876659710
PheGenIrs876659710
hapmaprs876659710
1000 genomesrs876659710
hgdprs876659710
ensemblrs876659710
gopubmedrs876659710
geneviewrs876659710
scholarrs876659710
googlers876659710
pharmgkbrs876659710
gwascentralrs876659710
openSNPrs876659710
23andMers876659710
23andMe allrs876659710
SNP Nexus

SNPshotrs876659710
SNPdbers876659710
MSV3drs876659710
GWAS Ctlgrs876659710
Max Magnitude0
ClinVar
Risk rs876659710(C;C)
Alt rs876659710(C;C)
Reference rs876659710(G;G)
Significance Probable-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.108128207G>C
CLNSRC
CLNACC RCV000223310.1,