rs2491132
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs2491132(C;T) |
Make rs2491132(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 30876800 |
Gene | SDC3 |
is a | snp |
is | mentioned by |
dbSNP | rs2491132 |
dbSNP (classic) | rs2491132 |
ClinGen | rs2491132 |
ebi | rs2491132 |
HLI | rs2491132 |
Exac | rs2491132 |
Gnomad | rs2491132 |
Varsome | rs2491132 |
LitVar | rs2491132 |
Map | rs2491132 |
PheGenI | rs2491132 |
Biobank | rs2491132 |
1000 genomes | rs2491132 |
hgdp | rs2491132 |
ensembl | rs2491132 |
geneview | rs2491132 |
scholar | rs2491132 |
rs2491132 | |
pharmgkb | rs2491132 |
gwascentral | rs2491132 |
openSNP | rs2491132 |
23andMe | rs2491132 |
SNPshot | rs2491132 |
SNPdbe | rs2491132 |
MSV3d | rs2491132 |
GWAS Ctlg | rs2491132 |
GMAF | 0.101 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs2491132(G;G) rs2491132(T;T) |
Alt | rs2491132(G;G) rs2491132(T;T) |
Reference | Rs2491132(C;C) |
Significance | Other |
Disease | Obesity |
Variation | info |
Gene | SDC3 |
CLNDBN | Obesity, association with |
Reversed | 0 |
HGVS | NC_000001.10:g.31349647C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000013593.17, |
[PMID 14606043] Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35.
[PMID 17018662] Positive association of obesity with single nucleotide polymorphisms of syndecan 3 in the Korean population.