Have questions? Visit https://www.reddit.com/r/SNPedia

rs267608073

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;AAG) 5 Variant of uncertain significance; possible Lynch syndrome mutation
(AAG;AAG) 0 common/normal


Make rs267608073(-;-)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position47801023
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608073
dbSNP (old)rs267608073
ClinGenrs267608073
ebirs267608073
HLIrs267608073
Exacrs267608073
Gnomadrs267608073
Varsomers267608073
LitVarrs267608073
Maprs267608073
PheGenIrs267608073
Biobankrs267608073
1000 genomesrs267608073
hgdprs267608073
ensemblrs267608073
gopubmedrs267608073
geneviewrs267608073
scholarrs267608073
googlers267608073
pharmgkbrs267608073
gwascentralrs267608073
openSNPrs267608073
23andMers267608073
23andMe allrs267608073
SNPshotrs267608073
SNPdbers267608073
MSV3drs267608073
GWAS Ctlgrs267608073
Max Magnitude5

c.3040_3042delAAG (p.Lys1014del); also reported in literature as 1013delCTT, c.3037_3039delAAG, and p.Lys1013del.

23andMe name: i5037885