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rs866771359

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs866771359(-;-)
Make rs866771359(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47806496
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs866771359
ebirs866771359
HLIrs866771359
Exacrs866771359
Varsomers866771359
Maprs866771359
PheGenIrs866771359
hapmaprs866771359
1000 genomesrs866771359
hgdprs866771359
ensemblrs866771359
gopubmedrs866771359
geneviewrs866771359
scholarrs866771359
googlers866771359
pharmgkbrs866771359
gwascentralrs866771359
openSNPrs866771359
23andMers866771359
23andMe allrs866771359
SNP Nexus

SNPshotrs866771359
SNPdbers866771359
MSV3drs866771359
GWAS Ctlgrs866771359
Max Magnitude0
ClinVar
Risk rs866771359(TATTA,TT;TATTA,TT)
Alt rs866771359(TATTA,TT;TATTA,TT)
Reference rs866771359(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.48033635dupT
CLNSRC
CLNACC RCV000216834.1,