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rs878853809

From SNPedia

Orientationplus
Geno Mag Summary
(CAGT;CAGT) 0 common in clinvar
Make rs878853809(-;-)
Make rs878853809(-;GTCA)
Make rs878853809(GTCA;GTCA)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47476511
GeneMSH2
is asnp
is mentioned by
dbSNPrs878853809
ebirs878853809
HLIrs878853809
Exacrs878853809
Varsomers878853809
Maprs878853809
PheGenIrs878853809
hapmaprs878853809
1000 genomesrs878853809
hgdprs878853809
ensemblrs878853809
gopubmedrs878853809
geneviewrs878853809
scholarrs878853809
googlers878853809
pharmgkbrs878853809
gwascentralrs878853809
openSNPrs878853809
23andMers878853809
23andMe allrs878853809
SNP Nexus

SNPshotrs878853809
SNPdbers878853809
MSV3drs878853809
GWAS Ctlgrs878853809
Max Magnitude0
ClinVar
Risk rs878853809(;)
Alt rs878853809(;)
Reference rs878853809(CAGT;CAGT)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703650_47703653delGTCA
CLNSRC
CLNACC RCV000234418.1,