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rs267608106

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;GGTA) 6 Lynch syndrome, pathogenic mutation
(GGTA;GGTA) 0 common in clinvar
(TAGG;TAGG) 0 common in clinvar


Make rs267608106(-;-)
ReferenceGRCh38 38.1/141
Chromosome2
Position47805707
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608106
dbSNP (classic)rs267608106
ClinGenrs267608106
ebirs267608106
HLIrs267608106
Exacrs267608106
Gnomadrs267608106
Varsomers267608106
LitVarrs267608106
Maprs267608106
PheGenIrs267608106
Biobankrs267608106
1000 genomesrs267608106
hgdprs267608106
ensemblrs267608106
geneviewrs267608106
scholarrs267608106
googlers267608106
pharmgkbrs267608106
gwascentralrs267608106
openSNPrs267608106
23andMers267608106
23andMe allrs267608106
SNPshotrs267608106
SNPdbers267608106
MSV3drs267608106
GWAS Ctlgrs267608106
Max Magnitude6

\

c.3646_3646+3del

23andMe name: i5037879

ClinVar
Risk rs267608106(-;-)
Alt rs267608106(-;-)
Reference Rs267608106(TAGG;TAGG)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48032846_48032849delGGTA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074901.3,