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rs121913660

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913660(C;T)
Make rs121913660(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67611511
GeneNDUFV1
is asnp
is mentioned by
dbSNPrs121913660
ebirs121913660
HLIrs121913660
Exacrs121913660
Varsomers121913660
Maprs121913660
PheGenIrs121913660
hapmaprs121913660
1000 genomesrs121913660
hgdprs121913660
ensemblrs121913660
gopubmedrs121913660
geneviewrs121913660
scholarrs121913660
googlers121913660
pharmgkbrs121913660
gwascentralrs121913660
openSNPrs121913660
23andMers121913660
23andMe allrs121913660
SNP Nexus

SNPshotrs121913660
SNPdbers121913660
MSV3drs121913660
GWAS Ctlgrs121913660
Max Magnitude0
OMIM161015
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121913660(T;T)
Alt rs121913660(T;T)
Reference rs121913660(C;C)
Significance Pathogenic
Disease Mitochondrial complex I deficiency
Variation info
Gene NDUFV1
CLNDBN Mitochondrial complex I deficiency
Reversed 0
HGVS NC_000011.9:g.67378982C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015102.26,