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rs398123231

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123231(A;A)
Make rs398123231(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47804948
GeneMSH6
is asnp
is mentioned by
dbSNPrs398123231
ebirs398123231
HLIrs398123231
Exacrs398123231
Varsomers398123231
Maprs398123231
PheGenIrs398123231
hapmaprs398123231
1000 genomesrs398123231
hgdprs398123231
ensemblrs398123231
gopubmedrs398123231
geneviewrs398123231
scholarrs398123231
googlers398123231
pharmgkbrs398123231
gwascentralrs398123231
openSNPrs398123231
23andMers398123231
23andMe allrs398123231
SNP Nexus

SNPshotrs398123231
SNPdbers398123231
MSV3drs398123231
GWAS Ctlgrs398123231
Max Magnitude0
ClinVar
Risk rs398123231(A,G,T;A,G,T)
Alt rs398123231(A,G,T;A,G,T)
Reference rs398123231(C;C)
Significance Pathogenic
Disease not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN not provided Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48032087C>A; NC_000002.11:g.48032087C>G; NC_000002.11:g.48032087C>T
CLNSRC HGMD International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000078315.5, RCV000228304.1, RCV000074863.2, RCV000165527.1,