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rs863225421

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225421(-;G)
Make rs863225421(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47798883
GeneMSH6
is asnp
is mentioned by
dbSNPrs863225421
ClinGenrs863225421
ebirs863225421
HLIrs863225421
Exacrs863225421
Varsomers863225421
Maprs863225421
PheGenIrs863225421
hapmaprs863225421
1000 genomesrs863225421
hgdprs863225421
ensemblrs863225421
gopubmedrs863225421
geneviewrs863225421
scholarrs863225421
googlers863225421
pharmgkbrs863225421
gwascentralrs863225421
openSNPrs863225421
23andMers863225421
23andMe allrs863225421
SNP Nexus

SNPshotrs863225421
SNPdbers863225421
MSV3drs863225421
GWAS Ctlgrs863225421
Max Magnitude0
ClinVar
Risk rs863225421(G;G)
Alt rs863225421(G;G)
Reference Rs863225421(-;-)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48026022dupG
CLNSRC
CLNACC RCV000202094.1, RCV000213447.2,