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rs768050261

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs768050261(C;T)
Make rs768050261(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position67608571
GeneC11orf72, NDUFV1
is asnp
is mentioned by
dbSNPrs768050261
ebirs768050261
HLIrs768050261
Exacrs768050261
Varsomers768050261
Maprs768050261
PheGenIrs768050261
hapmaprs768050261
1000 genomesrs768050261
hgdprs768050261
ensemblrs768050261
gopubmedrs768050261
geneviewrs768050261
scholarrs768050261
googlers768050261
pharmgkbrs768050261
gwascentralrs768050261
openSNPrs768050261
23andMers768050261
23andMe allrs768050261
SNP Nexus

SNPshotrs768050261
SNPdbers768050261
MSV3drs768050261
GWAS Ctlgrs768050261
Max Magnitude0
ClinVar
Risk rs768050261(T;T)
Alt rs768050261(T;T)
Reference rs768050261(C;C)
Significance Pathogenic
Disease Mitochondrial complex I deficiency
Variation info
Gene C11orf72 NDUFV1
CLNDBN Mitochondrial complex I deficiency
Reversed 0
HGVS NC_000011.9:g.67376042C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015101.23,