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rs878853815

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853815(G;T)
Make rs878853815(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47408529
GeneMSH2
is asnp
is mentioned by
dbSNPrs878853815
ebirs878853815
HLIrs878853815
Exacrs878853815
Varsomers878853815
Maprs878853815
PheGenIrs878853815
hapmaprs878853815
1000 genomesrs878853815
hgdprs878853815
ensemblrs878853815
gopubmedrs878853815
geneviewrs878853815
scholarrs878853815
googlers878853815
pharmgkbrs878853815
gwascentralrs878853815
openSNPrs878853815
23andMers878853815
23andMe allrs878853815
SNP Nexus

SNPshotrs878853815
SNPdbers878853815
MSV3drs878853815
GWAS Ctlgrs878853815
Max Magnitude0
ClinVar
Risk rs878853815(T;T)
Alt rs878853815(T;T)
Reference rs878853815(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635668G>T
CLNSRC
CLNACC RCV000228392.1,