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rs878853721

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs878853721(-;-)
Make rs878853721(-;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800787
GeneMSH6
is asnp
is mentioned by
dbSNPrs878853721
ebirs878853721
HLIrs878853721
Exacrs878853721
Varsomers878853721
Maprs878853721
PheGenIrs878853721
hapmaprs878853721
1000 genomesrs878853721
hgdprs878853721
ensemblrs878853721
gopubmedrs878853721
geneviewrs878853721
scholarrs878853721
googlers878853721
pharmgkbrs878853721
gwascentralrs878853721
openSNPrs878853721
23andMers878853721
23andMe allrs878853721
SNP Nexus

SNPshotrs878853721
SNPdbers878853721
MSV3drs878853721
GWAS Ctlgrs878853721
Max Magnitude0
ClinVar
Risk rs878853721(;)
Alt rs878853721(;)
Reference rs878853721(CT;CT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027926_48027927delCT
CLNSRC
CLNACC RCV000233999.1,