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rs863224833

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224833(-;T)
Make rs863224833(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47414388
GeneMSH2
is asnp
is mentioned by
dbSNPrs863224833
dbSNP (old)rs863224833
ClinGenrs863224833
ebirs863224833
HLIrs863224833
Exacrs863224833
Varsomers863224833
Maprs863224833
PheGenIrs863224833
Biobankrs863224833
1000 genomesrs863224833
hgdprs863224833
ensemblrs863224833
gopubmedrs863224833
geneviewrs863224833
scholarrs863224833
googlers863224833
pharmgkbrs863224833
gwascentralrs863224833
openSNPrs863224833
23andMers863224833
23andMe allrs863224833
SNP Nexus

SNPshotrs863224833
SNPdbers863224833
MSV3drs863224833
GWAS Ctlgrs863224833
Max Magnitude0
ClinVar
Risk rs863224833(T;T)
Alt rs863224833(T;T)
Reference Rs863224833(-;-)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47641527dupT
CLNSRC
CLNACC RCV000197610.1, RCV000485998.1,