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rs876658497

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658497(-;-)
Make rs876658497(-;AAGT)
Make rs876658497(AAGT;AAGT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47806784
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs876658497
ebirs876658497
HLIrs876658497
Exacrs876658497
Varsomers876658497
Maprs876658497
PheGenIrs876658497
hapmaprs876658497
1000 genomesrs876658497
hgdprs876658497
ensemblrs876658497
gopubmedrs876658497
geneviewrs876658497
scholarrs876658497
googlers876658497
pharmgkbrs876658497
gwascentralrs876658497
openSNPrs876658497
23andMers876658497
23andMe allrs876658497
SNP Nexus

SNPshotrs876658497
SNPdbers876658497
MSV3drs876658497
GWAS Ctlgrs876658497
Max Magnitude0
ClinVar
Risk rs876658497(AAGT;AAGT)
Alt rs876658497(AAGT;AAGT)
Reference rs876658497(;)
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.48033920_48033923dupAAGT
CLNSRC
CLNACC RCV000219545.1,