rs5937843
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs5937843(G;G) |
Make rs5937843(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 74529484 |
Gene | SLC16A2 |
is a | snp |
is | mentioned by |
dbSNP | rs5937843 |
dbSNP (classic) | rs5937843 |
ClinGen | rs5937843 |
ebi | rs5937843 |
HLI | rs5937843 |
Exac | rs5937843 |
Gnomad | rs5937843 |
Varsome | rs5937843 |
LitVar | rs5937843 |
Map | rs5937843 |
PheGenI | rs5937843 |
Biobank | rs5937843 |
1000 genomes | rs5937843 |
hgdp | rs5937843 |
ensembl | rs5937843 |
geneview | rs5937843 |
scholar | rs5937843 |
rs5937843 | |
pharmgkb | rs5937843 |
gwascentral | rs5937843 |
openSNP | rs5937843 |
23andMe | rs5937843 |
SNPshot | rs5937843 |
SNPdbe | rs5937843 |
MSV3d | rs5937843 |
GWAS Ctlg | rs5937843 |
GMAF | 0.4021 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 23978482] Associations between single nucleotide polymorphisms in thyroid hormone transporter genes (MCT8, MCT10 and OATP1C1) and circulating thyroid hormones
ClinVar | |
---|---|
Risk | rs5937843(G;G) |
Alt | rs5937843(G;G) |
Reference | Rs5937843(T;T) |
Significance | Probable-non-pathogenic |
Disease | not specified |
Variation | info |
Gene | SLC16A2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000023.10:g.73749319T>G |
CLNSRC | ClinVar University of Chicago |
CLNACC | RCV000147495.1, |
[PMID 31820424] Single Nucleotide Polymorphisms in Thyroid Hormone Transporter Genes MCT8, MCT10 and Deiodinase DIO2 Contribute to Inter-Individual Variance of Executive Functions and Personality Traits.