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rs201544686

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201544686(A;A)
Make rs201544686(A;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position73482209
GeneMTO1
is asnp
is mentioned by
dbSNPrs201544686
ebirs201544686
HLIrs201544686
Exacrs201544686
Varsomers201544686
Maprs201544686
PheGenIrs201544686
hapmaprs201544686
1000 genomesrs201544686
hgdprs201544686
ensemblrs201544686
gopubmedrs201544686
geneviewrs201544686
scholarrs201544686
googlers201544686
pharmgkbrs201544686
gwascentralrs201544686
openSNPrs201544686
23andMers201544686
23andMe allrs201544686
SNP Nexus

SNPshotrs201544686
SNPdbers201544686
MSV3drs201544686
GWAS Ctlgrs201544686
Max Magnitude0
ClinVar
Risk rs201544686(A;A)
Alt rs201544686(A;A)
Reference rs201544686(G;G)
Significance Pathogenic
Disease Combined oxidative phosphorylation deficiency 10 not provided
Variation info
Gene MTO1
CLNDBN Combined oxidative phosphorylation deficiency 10 not provided
Reversed 0
HGVS NC_000006.11:g.74191932G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000074506.2, RCV000224907.1,