rs376722149
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs376722149(C;T) |
Make rs376722149(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 47584422 |
Gene | NDUFS3 |
is a | snp |
is | mentioned by |
dbSNP | rs376722149 |
dbSNP (classic) | rs376722149 |
ClinGen | rs376722149 |
ebi | rs376722149 |
HLI | rs376722149 |
Exac | rs376722149 |
Gnomad | rs376722149 |
Varsome | rs376722149 |
LitVar | rs376722149 |
Map | rs376722149 |
PheGenI | rs376722149 |
Biobank | rs376722149 |
1000 genomes | rs376722149 |
hgdp | rs376722149 |
ensembl | rs376722149 |
geneview | rs376722149 |
scholar | rs376722149 |
rs376722149 | |
pharmgkb | rs376722149 |
gwascentral | rs376722149 |
openSNP | rs376722149 |
23andMe | rs376722149 |
SNPshot | rs376722149 |
SNPdbe | rs376722149 |
MSV3d | rs376722149 |
GWAS Ctlg | rs376722149 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs376722149(T;T) |
Alt | rs376722149(T;T) |
Reference | Rs376722149(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | NDUFS3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.47605974C>T |
CLNSRC | |
CLNACC | RCV000198333.2, |