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rs121434429

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121434429(C;C)
Make rs121434429(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position161213673
GeneFCER1G, NDUFS2
is asnp
is mentioned by
dbSNPrs121434429
ebirs121434429
HLIrs121434429
Exacrs121434429
Varsomers121434429
Maprs121434429
PheGenIrs121434429
hapmaprs121434429
1000 genomesrs121434429
hgdprs121434429
ensemblrs121434429
gopubmedrs121434429
geneviewrs121434429
scholarrs121434429
googlers121434429
pharmgkbrs121434429
gwascentralrs121434429
openSNPrs121434429
23andMers121434429
23andMe allrs121434429
SNP Nexus

SNPshotrs121434429
SNPdbers121434429
MSV3drs121434429
GWAS Ctlgrs121434429
Max Magnitude0
OMIM602985
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121434429(C;C)
Alt rs121434429(C;C)
Reference rs121434429(T;T)
Significance Pathogenic
Disease Mitochondrial complex I deficiency not provided
Variation info
Gene NDUFS2 FCER1G
CLNDBN Mitochondrial complex I deficiency not provided
Reversed 0
HGVS NC_000001.10:g.161183463T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000007103.2, RCV000199278.2,