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rs267606882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606882(A;A)
Make rs267606882(A;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position6264
GeneMT-TC
is asnp
is mentioned by
dbSNPrs267606882
ebirs267606882
HLIrs267606882
Exacrs267606882
Varsomers267606882
Maprs267606882
PheGenIrs267606882
hapmaprs267606882
1000 genomesrs267606882
hgdprs267606882
ensemblrs267606882
gopubmedrs267606882
geneviewrs267606882
scholarrs267606882
googlers267606882
pharmgkbrs267606882
gwascentralrs267606882
openSNPrs267606882
23andMers267606882
23andMe allrs267606882
SNP Nexus

SNPshotrs267606882
SNPdbers267606882
MSV3drs267606882
GWAS Ctlgrs267606882
Max Magnitude0
ClinVar
Risk rs267606882(A;A)
Alt rs267606882(A;A)
Reference rs267606882(G;G)
Significance Pathogenic
Disease Familial colorectal cancer
Variation info
Gene COX1
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_012920.1:m.6264G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010305.2,