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

rs267608062

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs267608062(-;-)
Make rs267608062(-;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47798828
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608062
ebirs267608062
HLIrs267608062
Exacrs267608062
Varsomers267608062
Maprs267608062
PheGenIrs267608062
hapmaprs267608062
1000 genomesrs267608062
hgdprs267608062
ensemblrs267608062
gopubmedrs267608062
geneviewrs267608062
scholarrs267608062
googlers267608062
pharmgkbrs267608062
gwascentralrs267608062
openSNPrs267608062
23andMers267608062
23andMe allrs267608062
SNP Nexus

SNPshotrs267608062
SNPdbers267608062
MSV3drs267608062
GWAS Ctlgrs267608062
Max Magnitude0
ClinVar
Risk rs267608062(TGGG,TT;TGGG,TT)
Alt rs267608062(TGGG,TT;TGGG,TT)
Reference rs267608062(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48025967dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075039.2,