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rs143747297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs143747297(A;A)
Make rs143747297(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position73482061
GeneMTO1
is asnp
is mentioned by
dbSNPrs143747297
ebirs143747297
HLIrs143747297
Exacrs143747297
Varsomers143747297
Maprs143747297
PheGenIrs143747297
hapmaprs143747297
1000 genomesrs143747297
hgdprs143747297
ensemblrs143747297
gopubmedrs143747297
geneviewrs143747297
scholarrs143747297
googlers143747297
pharmgkbrs143747297
gwascentralrs143747297
openSNPrs143747297
23andMers143747297
23andMe allrs143747297
SNP Nexus

SNPshotrs143747297
SNPdbers143747297
MSV3drs143747297
GWAS Ctlgrs143747297
Max Magnitude0
ClinVar
Risk rs143747297(A;A)
Alt rs143747297(A;A)
Reference rs143747297(G;G)
Significance Pathogenic
Disease Combined oxidative phosphorylation deficiency 10
Variation info
Gene MTO1
CLNDBN Combined oxidative phosphorylation deficiency 10
Reversed 0
HGVS NC_000006.11:g.74191784G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000029168.4,