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rs863225392

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225392(-;A)
Make rs863225392(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47478297
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225392
ClinGenrs863225392
ebirs863225392
HLIrs863225392
Exacrs863225392
Varsomers863225392
Maprs863225392
PheGenIrs863225392
hapmaprs863225392
1000 genomesrs863225392
hgdprs863225392
ensemblrs863225392
gopubmedrs863225392
geneviewrs863225392
scholarrs863225392
googlers863225392
pharmgkbrs863225392
gwascentralrs863225392
openSNPrs863225392
23andMers863225392
23andMe allrs863225392
SNP Nexus

SNPshotrs863225392
SNPdbers863225392
MSV3drs863225392
GWAS Ctlgrs863225392
Max Magnitude0
ClinVar
Risk rs863225392(A;A)
Alt rs863225392(A;A)
Reference Rs863225392(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47705436dupA
CLNSRC
CLNACC RCV000202169.1,