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rs876659872

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659872(C;T)
Make rs876659872(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108343240
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876659872
ebirs876659872
HLIrs876659872
Exacrs876659872
Varsomers876659872
Maprs876659872
PheGenIrs876659872
hapmaprs876659872
1000 genomesrs876659872
hgdprs876659872
ensemblrs876659872
gopubmedrs876659872
geneviewrs876659872
scholarrs876659872
googlers876659872
pharmgkbrs876659872
gwascentralrs876659872
openSNPrs876659872
23andMers876659872
23andMe allrs876659872
SNP Nexus

SNPshotrs876659872
SNPdbers876659872
MSV3drs876659872
GWAS Ctlgrs876659872
Max Magnitude0
ClinVar
Risk rs876659872(T;T)
Alt rs876659872(T;T)
Reference rs876659872(C;C)
Significance 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.108213967C>T
CLNSRC
CLNACC RCV000214803.1,