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rs267608076

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs267608076(-;-)
Make rs267608076(-;AG)
ReferenceGRCh38 38.1/141
Chromosome2
Position47799620
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608076
ebirs267608076
HLIrs267608076
Exacrs267608076
Varsomers267608076
Maprs267608076
PheGenIrs267608076
hapmaprs267608076
1000 genomesrs267608076
hgdprs267608076
ensemblrs267608076
gopubmedrs267608076
geneviewrs267608076
scholarrs267608076
googlers267608076
pharmgkbrs267608076
gwascentralrs267608076
openSNPrs267608076
23andMers267608076
23andMe allrs267608076
SNP Nexus

SNPshotrs267608076
SNPdbers267608076
MSV3drs267608076
GWAS Ctlgrs267608076
Max Magnitude0
ClinVar
Risk rs267608076(;)
Alt rs267608076(;)
Reference rs267608076(AG;AG)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH6
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48026759_48026760delAG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074676.2, RCV000217244.1,