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rs267608095

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608095(-;-)
Make rs267608095(-;T)
Make rs267608095(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47803520
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608095
ebirs267608095
HLIrs267608095
Exacrs267608095
Varsomers267608095
Maprs267608095
PheGenIrs267608095
hapmaprs267608095
1000 genomesrs267608095
hgdprs267608095
ensemblrs267608095
gopubmedrs267608095
geneviewrs267608095
scholarrs267608095
googlers267608095
pharmgkbrs267608095
gwascentralrs267608095
openSNPrs267608095
23andMers267608095
23andMe allrs267608095
SNP Nexus

SNPshotrs267608095
SNPdbers267608095
MSV3drs267608095
GWAS Ctlgrs267608095
Max Magnitude0
ClinVar
Risk rs267608095(T;T)
Alt rs267608095(T;T)
Reference rs267608095(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030659dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074834.2,