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rs267608063

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608063(-;-)
Make rs267608063(-;A)
Make rs267608063(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47800751
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608063
ebirs267608063
HLIrs267608063
Exacrs267608063
Varsomers267608063
Maprs267608063
PheGenIrs267608063
hapmaprs267608063
1000 genomesrs267608063
hgdprs267608063
ensemblrs267608063
gopubmedrs267608063
geneviewrs267608063
scholarrs267608063
googlers267608063
pharmgkbrs267608063
gwascentralrs267608063
openSNPrs267608063
23andMers267608063
23andMe allrs267608063
SNP Nexus

SNPshotrs267608063
SNPdbers267608063
MSV3drs267608063
GWAS Ctlgrs267608063
Max Magnitude0
ClinVar
Risk rs267608063(A;A)
Alt rs267608063(A;A)
Reference rs267608063(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027890dupA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074781.2,