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rs863225402

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225402(C;C)
Make rs863225402(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47790926
GeneMSH6
is asnp
is mentioned by
dbSNPrs863225402
ebirs863225402
HLIrs863225402
Exacrs863225402
Varsomers863225402
Maprs863225402
PheGenIrs863225402
hapmaprs863225402
1000 genomesrs863225402
hgdprs863225402
ensemblrs863225402
gopubmedrs863225402
geneviewrs863225402
scholarrs863225402
googlers863225402
pharmgkbrs863225402
gwascentralrs863225402
openSNPrs863225402
23andMers863225402
23andMe allrs863225402
SNP Nexus

SNPshotrs863225402
SNPdbers863225402
MSV3drs863225402
GWAS Ctlgrs863225402
Max Magnitude0
ClinVar
Risk rs863225402(C;C)
Alt rs863225402(C;C)
Reference rs863225402(G;G)
Significance Probable-Pathogenic
Disease not provided Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH6
CLNDBN not provided Lynch syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48018065G>C
CLNSRC
CLNACC RCV000202130.1, RCV000203910.1, RCV000222011.1,