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rs267608048

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608048(C;G)
Make rs267608048(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47798738
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608048
ebirs267608048
HLIrs267608048
Exacrs267608048
Varsomers267608048
Maprs267608048
PheGenIrs267608048
hapmaprs267608048
1000 genomesrs267608048
hgdprs267608048
ensemblrs267608048
gopubmedrs267608048
geneviewrs267608048
scholarrs267608048
googlers267608048
pharmgkbrs267608048
gwascentralrs267608048
openSNPrs267608048
23andMers267608048
23andMe allrs267608048
SNP Nexus

SNPshotrs267608048
SNPdbers267608048
MSV3drs267608048
GWAS Ctlgrs267608048
Max Magnitude0
ClinVar
Risk rs267608048(G;G)
Alt rs267608048(G;G)
Reference rs267608048(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48025877C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075035.2,