rs74315350
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs74315350(G;T) |
Make rs74315350(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 26912036 |
Gene | NR0B2, NUDC |
is a | snp |
is | mentioned by |
dbSNP | rs74315350 |
dbSNP (classic) | rs74315350 |
ClinGen | rs74315350 |
ebi | rs74315350 |
HLI | rs74315350 |
Exac | rs74315350 |
Gnomad | rs74315350 |
Varsome | rs74315350 |
LitVar | rs74315350 |
Map | rs74315350 |
PheGenI | rs74315350 |
Biobank | rs74315350 |
1000 genomes | rs74315350 |
hgdp | rs74315350 |
ensembl | rs74315350 |
geneview | rs74315350 |
scholar | rs74315350 |
rs74315350 | |
pharmgkb | rs74315350 |
gwascentral | rs74315350 |
openSNP | rs74315350 |
23andMe | rs74315350 |
SNPshot | rs74315350 |
SNPdbe | rs74315350 |
MSV3d | rs74315350 |
GWAS Ctlg | rs74315350 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs74315350(T;T) |
Alt | rs74315350(T;T) |
Reference | Rs74315350(G;G) |
Significance | Pathogenic |
Disease | Obesity |
Variation | info |
Gene | NR0B2 |
CLNDBN | Obesity, mild, early-onset |
Reversed | 1 |
HGVS | NC_000001.10:g.27238527C>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000005760.2, |