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rs863225387

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225387(C;T)
Make rs863225387(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47429902
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225387
ebirs863225387
HLIrs863225387
Exacrs863225387
Varsomers863225387
Maprs863225387
PheGenIrs863225387
hapmaprs863225387
1000 genomesrs863225387
hgdprs863225387
ensemblrs863225387
gopubmedrs863225387
geneviewrs863225387
scholarrs863225387
googlers863225387
pharmgkbrs863225387
gwascentralrs863225387
openSNPrs863225387
23andMers863225387
23andMe allrs863225387
SNP Nexus

SNPshotrs863225387
SNPdbers863225387
MSV3drs863225387
GWAS Ctlgrs863225387
Max Magnitude0
ClinVar
Risk rs863225387(T;T)
Alt rs863225387(T;T)
Reference rs863225387(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47657041C>T
CLNSRC
CLNACC RCV000202046.1,