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rs863225399

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225399(-;A)
Make rs863225399(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799295
GeneMSH6
is asnp
is mentioned by
dbSNPrs863225399
ClinGenrs863225399
ebirs863225399
HLIrs863225399
Exacrs863225399
Varsomers863225399
Maprs863225399
PheGenIrs863225399
hapmaprs863225399
1000 genomesrs863225399
hgdprs863225399
ensemblrs863225399
gopubmedrs863225399
geneviewrs863225399
scholarrs863225399
googlers863225399
pharmgkbrs863225399
gwascentralrs863225399
openSNPrs863225399
23andMers863225399
23andMe allrs863225399
SNP Nexus

SNPshotrs863225399
SNPdbers863225399
MSV3drs863225399
GWAS Ctlgrs863225399
Max Magnitude0
ClinVar
Risk rs863225399(A;A)
Alt rs863225399(A;A)
Reference Rs863225399(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48026434dupA
CLNSRC
CLNACC RCV000202043.1,