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rs267608083

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608083(-;-)
Make rs267608083(-;A)
Make rs267608083(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800062
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608083
ebirs267608083
HLIrs267608083
Exacrs267608083
Varsomers267608083
Maprs267608083
PheGenIrs267608083
hapmaprs267608083
1000 genomesrs267608083
hgdprs267608083
ensemblrs267608083
gopubmedrs267608083
geneviewrs267608083
scholarrs267608083
googlers267608083
pharmgkbrs267608083
gwascentralrs267608083
openSNPrs267608083
23andMers267608083
23andMe allrs267608083
SNP Nexus

SNPshotrs267608083
SNPdbers267608083
MSV3drs267608083
GWAS Ctlgrs267608083
Max Magnitude0
ClinVar
Risk rs267608083(A;A)
Alt rs267608083(A;A)
Reference rs267608083(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Lynch syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027201dupA
CLNSRC
CLNACC RCV000167251.1, RCV000210176.1,