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rs267608092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs267608092(-;-)
Make rs267608092(-;TT)
ReferenceGRCh38 38.1/141
Chromosome2
Position47803558
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608092
ebirs267608092
HLIrs267608092
Exacrs267608092
Varsomers267608092
Maprs267608092
PheGenIrs267608092
hapmaprs267608092
1000 genomesrs267608092
hgdprs267608092
ensemblrs267608092
gopubmedrs267608092
geneviewrs267608092
scholarrs267608092
googlers267608092
pharmgkbrs267608092
gwascentralrs267608092
openSNPrs267608092
23andMers267608092
23andMe allrs267608092
SNP Nexus

SNPshotrs267608092
SNPdbers267608092
MSV3drs267608092
GWAS Ctlgrs267608092
Max Magnitude0
ClinVar
Risk rs267608092(;)
Alt rs267608092(;)
Reference rs267608092(TT;TT)
Significance Pathogenic
Disease Hereditary nonpolyposis colorectal cancer type 5 Lynch syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MSH6
CLNDBN Hereditary nonpolyposis colorectal cancer type 5 Lynch syndrome not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000002.11:g.48030697_48030698delTT
CLNSRC International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC RCV000009490.6, RCV000074837.2, RCV000202034.1, RCV000223509.1,