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rs587779192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;C) 6 Lynch syndrome, pathogenic mutation
(C;C) 0 common in clinvar


Make rs587779192(-;-)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47414364
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779192
dbSNP (classic)rs587779192
ClinGenrs587779192
ebirs587779192
HLIrs587779192
Exacrs587779192
Gnomadrs587779192
Varsomers587779192
LitVarrs587779192
Maprs587779192
PheGenIrs587779192
Biobankrs587779192
1000 genomesrs587779192
hgdprs587779192
ensemblrs587779192
geneviewrs587779192
scholarrs587779192
googlers587779192
pharmgkbrs587779192
gwascentralrs587779192
openSNPrs587779192
23andMers587779192
SNPshotrs587779192
SNPdbers587779192
MSV3drs587779192
GWAS Ctlgrs587779192
Max Magnitude6
ClinVar
Risk rs587779192(-;-)
Alt rs587779192(-;-)
Reference Rs587779192(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641503delC
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076743.2,