rs17848368
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(G;G) | 0 |
Make rs17848368(C;T) |
Make rs17848368(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 74006298 |
Gene | UCP3 |
is a | snp |
is | mentioned by |
dbSNP | rs17848368 |
dbSNP (classic) | rs17848368 |
ClinGen | rs17848368 |
ebi | rs17848368 |
HLI | rs17848368 |
Exac | rs17848368 |
Gnomad | rs17848368 |
Varsome | rs17848368 |
LitVar | rs17848368 |
Map | rs17848368 |
PheGenI | rs17848368 |
Biobank | rs17848368 |
1000 genomes | rs17848368 |
hgdp | rs17848368 |
ensembl | rs17848368 |
geneview | rs17848368 |
scholar | rs17848368 |
rs17848368 | |
pharmgkb | rs17848368 |
gwascentral | rs17848368 |
openSNP | rs17848368 |
23andMe | rs17848368 |
SNPshot | rs17848368 |
SNPdbe | rs17848368 |
MSV3d | rs17848368 |
GWAS Ctlg | rs17848368 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs17848368(T;T) |
Alt | rs17848368(T;T) |
Reference | Rs17848368(C;C) |
Significance | Pathogenic |
Disease | Obesity |
Variation | info |
Gene | UCP3 |
CLNDBN | Obesity, severe, and type II diabetes |
Reversed | 1 |
HGVS | NC_000011.9:g.73717343G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000008017.1, |