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rs398123232

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs398123232(-;-)
Make rs398123232(-;AG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47804987
GeneMSH6
is asnp
is mentioned by
dbSNPrs398123232
ebirs398123232
HLIrs398123232
Exacrs398123232
Varsomers398123232
Maprs398123232
PheGenIrs398123232
hapmaprs398123232
1000 genomesrs398123232
hgdprs398123232
ensemblrs398123232
gopubmedrs398123232
geneviewrs398123232
scholarrs398123232
googlers398123232
pharmgkbrs398123232
gwascentralrs398123232
openSNPrs398123232
23andMers398123232
23andMe allrs398123232
SNP Nexus

SNPshotrs398123232
SNPdbers398123232
MSV3drs398123232
GWAS Ctlgrs398123232
Max Magnitude0
ClinVar
Risk rs398123232(;)
Alt rs398123232(;)
Reference rs398123232(AG;AG)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MSH6
CLNDBN not provided Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48032126_48032127delAG
CLNSRC HGMD
CLNACC RCV000078316.4, RCV000162479.1, RCV000200371.1,