rs142609245
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs142609245(C;C) |
Make rs142609245(C;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 201078946 |
Gene | NDUFB3 |
is a | snp |
is | mentioned by |
dbSNP | rs142609245 |
dbSNP (classic) | rs142609245 |
ClinGen | rs142609245 |
ebi | rs142609245 |
HLI | rs142609245 |
Exac | rs142609245 |
Gnomad | rs142609245 |
Varsome | rs142609245 |
LitVar | rs142609245 |
Map | rs142609245 |
PheGenI | rs142609245 |
Biobank | rs142609245 |
1000 genomes | rs142609245 |
hgdp | rs142609245 |
ensembl | rs142609245 |
geneview | rs142609245 |
scholar | rs142609245 |
rs142609245 | |
pharmgkb | rs142609245 |
gwascentral | rs142609245 |
openSNP | rs142609245 |
23andMe | rs142609245 |
SNPshot | rs142609245 |
SNPdbe | rs142609245 |
MSV3d | rs142609245 |
GWAS Ctlg | rs142609245 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs142609245(C;C) |
Alt | rs142609245(C;C) |
Reference | Rs142609245(T;T) |
Significance | Other |
Disease | not provided |
Variation | info |
Gene | NDUFB3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000002.11:g.201943669T>C |
CLNSRC | |
CLNACC | RCV000239318.2, |