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rs878853824

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853824(C;T)
Make rs878853824(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47412558
GeneMSH2
is asnp
is mentioned by
dbSNPrs878853824
ebirs878853824
HLIrs878853824
Exacrs878853824
Varsomers878853824
Maprs878853824
PheGenIrs878853824
hapmaprs878853824
1000 genomesrs878853824
hgdprs878853824
ensemblrs878853824
gopubmedrs878853824
geneviewrs878853824
scholarrs878853824
googlers878853824
pharmgkbrs878853824
gwascentralrs878853824
openSNPrs878853824
23andMers878853824
23andMe allrs878853824
SNP Nexus

SNPshotrs878853824
SNPdbers878853824
MSV3drs878853824
GWAS Ctlgrs878853824
Max Magnitude0
ClinVar
Risk rs878853824(T;T)
Alt rs878853824(T;T)
Reference rs878853824(C;C)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47639697C>T
CLNSRC
CLNACC RCV000233889.1, RCV000235710.1,