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rs878853739

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853739(-;-)
Make rs878853739(-;A)
Make rs878853739(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47806514
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs878853739
ebirs878853739
HLIrs878853739
Exacrs878853739
Varsomers878853739
Maprs878853739
PheGenIrs878853739
hapmaprs878853739
1000 genomesrs878853739
hgdprs878853739
ensemblrs878853739
gopubmedrs878853739
geneviewrs878853739
scholarrs878853739
googlers878853739
pharmgkbrs878853739
gwascentralrs878853739
openSNPrs878853739
23andMers878853739
23andMe allrs878853739
SNP Nexus

SNPshotrs878853739
SNPdbers878853739
MSV3drs878853739
GWAS Ctlgrs878853739
Max Magnitude0
ClinVar
Risk rs878853739(A;A)
Alt rs878853739(A;A)
Reference rs878853739(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033653dupA
CLNSRC
CLNACC RCV000230977.1,