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rs876659235

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659235(-;-)
Make rs876659235(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position108365342
GeneATM, C11orf65
is asnp
is mentioned by
dbSNPrs876659235
ebirs876659235
HLIrs876659235
Exacrs876659235
Varsomers876659235
Maprs876659235
PheGenIrs876659235
hapmaprs876659235
1000 genomesrs876659235
hgdprs876659235
ensemblrs876659235
gopubmedrs876659235
geneviewrs876659235
scholarrs876659235
googlers876659235
pharmgkbrs876659235
gwascentralrs876659235
openSNPrs876659235
23andMers876659235
23andMe allrs876659235
SNP Nexus

SNPshotrs876659235
SNPdbers876659235
MSV3drs876659235
GWAS Ctlgrs876659235
Max Magnitude0
ClinVar
Risk rs876659235(;)
Alt rs876659235(;)
Reference rs876659235(T;T)
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.108236069delT
CLNSRC
CLNACC RCV000219949.1,