Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606884

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606884(C;C)
Make rs267606884(C;T)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position7275
GeneMT-ATP6
is asnp
is mentioned by
dbSNPrs267606884
ebirs267606884
HLIrs267606884
Exacrs267606884
Varsomers267606884
Maprs267606884
PheGenIrs267606884
hapmaprs267606884
1000 genomesrs267606884
hgdprs267606884
ensemblrs267606884
gopubmedrs267606884
geneviewrs267606884
scholarrs267606884
googlers267606884
pharmgkbrs267606884
gwascentralrs267606884
openSNPrs267606884
23andMers267606884
23andMe allrs267606884
SNP Nexus

SNPshotrs267606884
SNPdbers267606884
MSV3drs267606884
GWAS Ctlgrs267606884
Max Magnitude0
ClinVar
Risk rs267606884(C;C)
Alt rs267606884(C;C)
Reference rs267606884(T;T)
Significance Pathogenic
Disease Familial colorectal cancer
Variation info
Gene COX1
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_012920.1:m.7275T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010311.4,