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rs863225397

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225397(A;A)
Make rs863225397(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47414268
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225397
ebirs863225397
HLIrs863225397
Exacrs863225397
Varsomers863225397
Maprs863225397
PheGenIrs863225397
hapmaprs863225397
1000 genomesrs863225397
hgdprs863225397
ensemblrs863225397
gopubmedrs863225397
geneviewrs863225397
scholarrs863225397
googlers863225397
pharmgkbrs863225397
gwascentralrs863225397
openSNPrs863225397
23andMers863225397
23andMe allrs863225397
SNP Nexus

SNPshotrs863225397
SNPdbers863225397
MSV3drs863225397
GWAS Ctlgrs863225397
Max Magnitude0
ClinVar
Risk rs863225397(A;A)
Alt rs863225397(A;A)
Reference rs863225397(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47641407G>A
CLNSRC
CLNACC RCV000202050.1,