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rs876658957

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658957(G;T)
Make rs876658957(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108335962
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876658957
ebirs876658957
HLIrs876658957
Exacrs876658957
Varsomers876658957
Maprs876658957
PheGenIrs876658957
hapmaprs876658957
1000 genomesrs876658957
hgdprs876658957
ensemblrs876658957
gopubmedrs876658957
geneviewrs876658957
scholarrs876658957
googlers876658957
pharmgkbrs876658957
gwascentralrs876658957
openSNPrs876658957
23andMers876658957
23andMe allrs876658957
SNP Nexus

SNPshotrs876658957
SNPdbers876658957
MSV3drs876658957
GWAS Ctlgrs876658957
Max Magnitude0
ClinVar
Risk rs876658957(T;T)
Alt rs876658957(T;T)
Reference rs876658957(G;G)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene C11orf65 ATM
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000011.9:g.108206689G>T
CLNSRC
CLNACC RCV000220293.1,