Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853709

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853709(-;-)
Make rs878853709(-;C)
Make rs878853709(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47799553
GeneMSH6
is asnp
is mentioned by
dbSNPrs878853709
ebirs878853709
HLIrs878853709
Exacrs878853709
Varsomers878853709
Maprs878853709
PheGenIrs878853709
hapmaprs878853709
1000 genomesrs878853709
hgdprs878853709
ensemblrs878853709
gopubmedrs878853709
geneviewrs878853709
scholarrs878853709
googlers878853709
pharmgkbrs878853709
gwascentralrs878853709
openSNPrs878853709
23andMers878853709
23andMe allrs878853709
SNP Nexus

SNPshotrs878853709
SNPdbers878853709
MSV3drs878853709
GWAS Ctlgrs878853709
Max Magnitude0
ClinVar
Risk rs878853709(C;C)
Alt rs878853709(C;C)
Reference rs878853709(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026692_48026693insC
CLNSRC
CLNACC RCV000231145.1,