rs2304796
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2304796(C;T) |
Make rs2304796(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 89667026 |
Gene | PLIN1 |
is a | snp |
is | mentioned by |
dbSNP | rs2304796 |
dbSNP (classic) | rs2304796 |
ClinGen | rs2304796 |
ebi | rs2304796 |
HLI | rs2304796 |
Exac | rs2304796 |
Gnomad | rs2304796 |
Varsome | rs2304796 |
LitVar | rs2304796 |
Map | rs2304796 |
PheGenI | rs2304796 |
Biobank | rs2304796 |
1000 genomes | rs2304796 |
hgdp | rs2304796 |
ensembl | rs2304796 |
geneview | rs2304796 |
scholar | rs2304796 |
rs2304796 | |
pharmgkb | rs2304796 |
gwascentral | rs2304796 |
openSNP | rs2304796 |
23andMe | rs2304796 |
SNPshot | rs2304796 |
SNPdbe | rs2304796 |
MSV3d | rs2304796 |
GWAS Ctlg | rs2304796 |
Max Magnitude | 0 |
[PMID 23517113] Association between three genetic variants of the Perilipin Gene (PLIN) and glucose metabolism: results from a replication study among Chinese adults and a meta-analysis
ClinVar | |
---|---|
Risk | rs2304796(G;G) rs2304796(T;T) |
Alt | rs2304796(G;G) rs2304796(T;T) |
Reference | Rs2304796(C;C) |
Significance | Probable-non-pathogenic |
Disease | not specified |
Variation | info |
Gene | PLIN1 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000015.9:g.90210257G>A |
CLNSRC | ClinVar University of Chicago |
CLNACC | RCV000117992.2, |