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rs863225395

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225395(C;G)
Make rs863225395(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47478361
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225395
ebirs863225395
HLIrs863225395
Exacrs863225395
Varsomers863225395
Maprs863225395
PheGenIrs863225395
hapmaprs863225395
1000 genomesrs863225395
hgdprs863225395
ensemblrs863225395
gopubmedrs863225395
geneviewrs863225395
scholarrs863225395
googlers863225395
pharmgkbrs863225395
gwascentralrs863225395
openSNPrs863225395
23andMers863225395
23andMe allrs863225395
SNP Nexus

SNPshotrs863225395
SNPdbers863225395
MSV3drs863225395
GWAS Ctlgrs863225395
Max Magnitude0
ClinVar
Risk rs863225395(G;G)
Alt rs863225395(G;G)
Reference rs863225395(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47705500C>G
CLNSRC
CLNACC RCV000202080.1,