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rs863224474

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863224474(-;T)
Make rs863224474(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47799727
GeneMSH6
is asnp
is mentioned by
dbSNPrs863224474
dbSNP (old)rs863224474
ClinGenrs863224474
ebirs863224474
HLIrs863224474
Exacrs863224474
Gnomadrs863224474
Varsomers863224474
Maprs863224474
PheGenIrs863224474
Biobankrs863224474
1000 genomesrs863224474
hgdprs863224474
ensemblrs863224474
gopubmedrs863224474
geneviewrs863224474
scholarrs863224474
googlers863224474
pharmgkbrs863224474
gwascentralrs863224474
openSNPrs863224474
23andMers863224474
23andMe allrs863224474
SNP Nexus

SNPshotrs863224474
SNPdbers863224474
MSV3drs863224474
GWAS Ctlgrs863224474
Max Magnitude0
ClinVar
Risk rs863224474(T;T)
Alt rs863224474(T;T)
Reference Rs863224474(-;-)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026866dupT
CLNSRC
CLNACC RCV000195900.1,