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rs876658817

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658817(-;-)
Make rs876658817(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47806532
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs876658817
ebirs876658817
HLIrs876658817
Exacrs876658817
Varsomers876658817
Maprs876658817
PheGenIrs876658817
hapmaprs876658817
1000 genomesrs876658817
hgdprs876658817
ensemblrs876658817
gopubmedrs876658817
geneviewrs876658817
scholarrs876658817
googlers876658817
pharmgkbrs876658817
gwascentralrs876658817
openSNPrs876658817
23andMers876658817
23andMe allrs876658817
SNP Nexus

SNPshotrs876658817
SNPdbers876658817
MSV3drs876658817
GWAS Ctlgrs876658817
Max Magnitude0
ClinVar
Risk rs876658817(;)
Alt rs876658817(;)
Reference rs876658817(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene FBXO11 MSH6
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48033671delT
CLNSRC
CLNACC RCV000214257.1,