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rs199474826

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199474826(A;A)
Make rs199474826(A;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position8009
GeneMT-ATP6
is asnp
is mentioned by
dbSNPrs199474826
ebirs199474826
HLIrs199474826
Exacrs199474826
Varsomers199474826
Maprs199474826
PheGenIrs199474826
hapmaprs199474826
1000 genomesrs199474826
hgdprs199474826
ensemblrs199474826
gopubmedrs199474826
geneviewrs199474826
scholarrs199474826
googlers199474826
pharmgkbrs199474826
gwascentralrs199474826
openSNPrs199474826
23andMers199474826
23andMe allrs199474826
SNP Nexus

SNPshotrs199474826
SNPdbers199474826
MSV3drs199474826
GWAS Ctlgrs199474826
Max Magnitude0
ClinVar
Risk rs199474826(A;A)
Alt rs199474826(A;A)
Reference rs199474826(G;G)
Significance Pathogenic
Disease Familial colorectal cancer
Variation info
Gene COX2
CLNDBN Familial colorectal cancer
Reversed 0
HGVS NC_012920.1:m.8009G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010295.2,