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rs267608077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGAG;AAGAG) 0 common in clinvar
(AGAGA;AGAGA) 0 common in clinvar
Make rs267608077(-;-)
Make rs267608077(-;AGAGA)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799118
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608077
ebirs267608077
HLIrs267608077
Exacrs267608077
Varsomers267608077
Maprs267608077
PheGenIrs267608077
hapmaprs267608077
1000 genomesrs267608077
hgdprs267608077
ensemblrs267608077
gopubmedrs267608077
geneviewrs267608077
scholarrs267608077
googlers267608077
pharmgkbrs267608077
gwascentralrs267608077
openSNPrs267608077
23andMers267608077
23andMe allrs267608077
SNP Nexus

SNPshotrs267608077
SNPdbers267608077
MSV3drs267608077
GWAS Ctlgrs267608077
Max Magnitude0
ClinVar
Risk rs267608077(;)
Alt rs267608077(;)
Reference rs267608077(AAGAG;AAGAG)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48026257_48026261delAGAGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074635.2, RCV000129834.3, RCV000202120.1,