rs146407178
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs146407178(C;T) |
Make rs146407178(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 47582130 |
Gene | NDUFS3 |
is a | snp |
is | mentioned by |
dbSNP | rs146407178 |
dbSNP (classic) | rs146407178 |
ClinGen | rs146407178 |
ebi | rs146407178 |
HLI | rs146407178 |
Exac | rs146407178 |
Gnomad | rs146407178 |
Varsome | rs146407178 |
LitVar | rs146407178 |
Map | rs146407178 |
PheGenI | rs146407178 |
Biobank | rs146407178 |
1000 genomes | rs146407178 |
hgdp | rs146407178 |
ensembl | rs146407178 |
geneview | rs146407178 |
scholar | rs146407178 |
rs146407178 | |
pharmgkb | rs146407178 |
gwascentral | rs146407178 |
openSNP | rs146407178 |
23andMe | rs146407178 |
SNPshot | rs146407178 |
SNPdbe | rs146407178 |
MSV3d | rs146407178 |
GWAS Ctlg | rs146407178 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs146407178(T;T) |
Alt | rs146407178(T;T) |
Reference | Rs146407178(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | NDUFS3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.47603682C>T |
CLNSRC | |
CLNACC | RCV000489564.1, |