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rs878853718

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853718(C;T)
Make rs878853718(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800663
GeneMSH6
is asnp
is mentioned by
dbSNPrs878853718
ebirs878853718
HLIrs878853718
Exacrs878853718
Varsomers878853718
Maprs878853718
PheGenIrs878853718
hapmaprs878853718
1000 genomesrs878853718
hgdprs878853718
ensemblrs878853718
gopubmedrs878853718
geneviewrs878853718
scholarrs878853718
googlers878853718
pharmgkbrs878853718
gwascentralrs878853718
openSNPrs878853718
23andMers878853718
23andMe allrs878853718
SNP Nexus

SNPshotrs878853718
SNPdbers878853718
MSV3drs878853718
GWAS Ctlgrs878853718
Max Magnitude0
ClinVar
Risk rs878853718(T;T)
Alt rs878853718(T;T)
Reference rs878853718(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027802C>T
CLNSRC
CLNACC RCV000232801.1,