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rs878853745

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853745(A;G)
Make rs878853745(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47806777
GeneFBXO11, MSH6
is asnp
is mentioned by
dbSNPrs878853745
ebirs878853745
HLIrs878853745
Exacrs878853745
Varsomers878853745
Maprs878853745
PheGenIrs878853745
hapmaprs878853745
1000 genomesrs878853745
hgdprs878853745
ensemblrs878853745
gopubmedrs878853745
geneviewrs878853745
scholarrs878853745
googlers878853745
pharmgkbrs878853745
gwascentralrs878853745
openSNPrs878853745
23andMers878853745
23andMe allrs878853745
SNP Nexus

SNPshotrs878853745
SNPdbers878853745
MSV3drs878853745
GWAS Ctlgrs878853745
Max Magnitude0
ClinVar
Risk rs878853745(G;G)
Alt rs878853745(G;G)
Reference rs878853745(A;A)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene FBXO11 MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033916A>G
CLNSRC
CLNACC RCV000231436.1,