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rs863225406

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs863225406(-;-)
Make rs863225406(-;CT)
Make rs863225406(CT;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47803485
GeneMSH6
is asnp
is mentioned by
dbSNPrs863225406
ClinGenrs863225406
ebirs863225406
HLIrs863225406
Exacrs863225406
Varsomers863225406
Maprs863225406
PheGenIrs863225406
hapmaprs863225406
1000 genomesrs863225406
hgdprs863225406
ensemblrs863225406
gopubmedrs863225406
geneviewrs863225406
scholarrs863225406
googlers863225406
pharmgkbrs863225406
gwascentralrs863225406
openSNPrs863225406
23andMers863225406
23andMe allrs863225406
SNP Nexus

SNPshotrs863225406
SNPdbers863225406
MSV3drs863225406
GWAS Ctlgrs863225406
Max Magnitude0
ClinVar
Risk rs863225406(-;-)
Alt rs863225406(-;-)
Reference Rs863225406(TC;TC)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH6
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.48030624_48030625delCT
CLNSRC
CLNACC RCV000201961.1,