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rs267608114

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs267608114(-;-)
Make rs267608114(-;AT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47806356
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608114
ebirs267608114
HLIrs267608114
Exacrs267608114
Varsomers267608114
Maprs267608114
PheGenIrs267608114
hapmaprs267608114
1000 genomesrs267608114
hgdprs267608114
ensemblrs267608114
gopubmedrs267608114
geneviewrs267608114
scholarrs267608114
googlers267608114
pharmgkbrs267608114
gwascentralrs267608114
openSNPrs267608114
23andMers267608114
23andMe allrs267608114
SNP Nexus

SNPshotrs267608114
SNPdbers267608114
MSV3drs267608114
GWAS Ctlgrs267608114
Max Magnitude0
ClinVar
Risk rs267608114(;)
Alt rs267608114(;)
Reference rs267608114(AT;AT)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH6
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48033495_48033496delAT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074931.2, RCV000202066.1,