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rs876658223

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 6 Lynch syndrome
Make rs876658223(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47463034
GeneMSH2
is asnp
is mentioned by
dbSNPrs876658223
dbSNP (classic)rs876658223
ClinGenrs876658223
ebirs876658223
HLIrs876658223
Exacrs876658223
Gnomadrs876658223
Varsomers876658223
LitVarrs876658223
Maprs876658223
PheGenIrs876658223
Biobankrs876658223
1000 genomesrs876658223
hgdprs876658223
ensemblrs876658223
geneviewrs876658223
scholarrs876658223
googlers876658223
pharmgkbrs876658223
gwascentralrs876658223
openSNPrs876658223
23andMers876658223
SNPshotrs876658223
SNPdbers876658223
MSV3drs876658223
GWAS Ctlgrs876658223
Max Magnitude6
ClinVar
Risk rs876658223(T;T)
Alt rs876658223(T;T)
Reference Rs876658223(G;G)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47690173G>T
CLNSRC
CLNACC RCV000215886.1,