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rs267608088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608088(-;-)
Make rs267608088(-;T)
Make rs267608088(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47803571
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608088
ebirs267608088
HLIrs267608088
Exacrs267608088
Varsomers267608088
Maprs267608088
PheGenIrs267608088
hapmaprs267608088
1000 genomesrs267608088
hgdprs267608088
ensemblrs267608088
gopubmedrs267608088
geneviewrs267608088
scholarrs267608088
googlers267608088
pharmgkbrs267608088
gwascentralrs267608088
openSNPrs267608088
23andMers267608088
23andMe allrs267608088
SNP Nexus

SNPshotrs267608088
SNPdbers267608088
MSV3drs267608088
GWAS Ctlgrs267608088
Max Magnitude0
ClinVar
Risk rs267608088(T;T)
Alt rs267608088(T;T)
Reference rs267608088(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48030710dupT
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074840.2,