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rs13424612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs13424612(C;T)
Make rs13424612(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position239960704
GeneNDUFA10
is asnp
is mentioned by
dbSNPrs13424612
dbSNP (old)rs13424612
ClinGenrs13424612
ebirs13424612
HLIrs13424612
Exacrs13424612
Varsomers13424612
Maprs13424612
PheGenIrs13424612
Biobankrs13424612
1000 genomesrs13424612
hgdprs13424612
ensemblrs13424612
gopubmedrs13424612
geneviewrs13424612
scholarrs13424612
googlers13424612
pharmgkbrs13424612
gwascentralrs13424612
openSNPrs13424612
23andMers13424612
23andMe allrs13424612
SNP Nexus

SNPshotrs13424612
SNPdbers13424612
MSV3drs13424612
GWAS Ctlgrs13424612
GMAF0.3095
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23910658]
Trait Odorant perception
Title Identification of regions associated with variation in sensitivity to food-related odors in the human genome.
Risk Allele
P-val 6E-10
Odds Ratio 6.62 [NR] unit increase


ClinVar
Risk rs13424612(T;T)
Alt rs13424612(T;T)
Reference Rs13424612(C;C)
Significance Probable-non-pathogenic
Disease Leigh syndrome Mitochondrial complex I deficiency
Variation info
Gene NDUFA10
CLNDBN Leigh syndrome Mitochondrial complex I deficiency
Reversed 0
HGVS NC_000002.11:g.240900121C>T
CLNSRC
CLNACC RCV000345516.1, RCV000408266.1,