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rs281865417

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865417(A;A)
Make rs281865417(A;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position6277
GeneMT-TC
is asnp
is mentioned by
dbSNPrs281865417
ebirs281865417
HLIrs281865417
Exacrs281865417
Varsomers281865417
Maprs281865417
PheGenIrs281865417
hapmaprs281865417
1000 genomesrs281865417
hgdprs281865417
ensemblrs281865417
gopubmedrs281865417
geneviewrs281865417
scholarrs281865417
googlers281865417
pharmgkbrs281865417
gwascentralrs281865417
openSNPrs281865417
23andMers281865417
23andMe allrs281865417
SNP Nexus

SNPshotrs281865417
SNPdbers281865417
MSV3drs281865417
GWAS Ctlgrs281865417
Max Magnitude0
ClinVar
Risk rs281865417(A;A)
Alt rs281865417(A;A)
Reference rs281865417(G;G)
Significance Pathogenic
Disease Familial colorectal cancer
Variation info
Gene COX1
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_012920.1:m.6277G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010310.2,