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rs878853729

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853729(-;-)
Make rs878853729(-;G)
Make rs878853729(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47801146
GeneMSH6
is asnp
is mentioned by
dbSNPrs878853729
ebirs878853729
HLIrs878853729
Exacrs878853729
Varsomers878853729
Maprs878853729
PheGenIrs878853729
hapmaprs878853729
1000 genomesrs878853729
hgdprs878853729
ensemblrs878853729
gopubmedrs878853729
geneviewrs878853729
scholarrs878853729
googlers878853729
pharmgkbrs878853729
gwascentralrs878853729
openSNPrs878853729
23andMers878853729
23andMe allrs878853729
SNP Nexus

SNPshotrs878853729
SNPdbers878853729
MSV3drs878853729
GWAS Ctlgrs878853729
Max Magnitude0
ClinVar
Risk rs878853729(G;G)
Alt rs878853729(G;G)
Reference rs878853729(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48028285dupG
CLNSRC
CLNACC RCV000233953.1,