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rs863224473

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224473(C;T)
Make rs863224473(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799028
GeneMSH6
is asnp
is mentioned by
dbSNPrs863224473
ebirs863224473
HLIrs863224473
Exacrs863224473
Varsomers863224473
Maprs863224473
PheGenIrs863224473
hapmaprs863224473
1000 genomesrs863224473
hgdprs863224473
ensemblrs863224473
gopubmedrs863224473
geneviewrs863224473
scholarrs863224473
googlers863224473
pharmgkbrs863224473
gwascentralrs863224473
openSNPrs863224473
23andMers863224473
23andMe allrs863224473
SNP Nexus

SNPshotrs863224473
SNPdbers863224473
MSV3drs863224473
GWAS Ctlgrs863224473
Max Magnitude0
ClinVar
Risk rs863224473(T;T)
Alt rs863224473(T;T)
Reference rs863224473(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026167C>T
CLNSRC
CLNACC RCV000196898.1,