rs13424612
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs13424612(C;T) |
Make rs13424612(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 239960704 |
Gene | NDUFA10 |
is a | snp |
is | mentioned by |
dbSNP | rs13424612 |
dbSNP (classic) | rs13424612 |
ClinGen | rs13424612 |
ebi | rs13424612 |
HLI | rs13424612 |
Exac | rs13424612 |
Gnomad | rs13424612 |
Varsome | rs13424612 |
LitVar | rs13424612 |
Map | rs13424612 |
PheGenI | rs13424612 |
Biobank | rs13424612 |
1000 genomes | rs13424612 |
hgdp | rs13424612 |
ensembl | rs13424612 |
geneview | rs13424612 |
scholar | rs13424612 |
rs13424612 | |
pharmgkb | rs13424612 |
gwascentral | rs13424612 |
openSNP | rs13424612 |
23andMe | rs13424612 |
SNPshot | rs13424612 |
SNPdbe | rs13424612 |
MSV3d | rs13424612 |
GWAS Ctlg | rs13424612 |
GMAF | 0.3095 |
Max Magnitude | 0 |
? | (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, |