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rs5937843

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs5937843(G;G)
Make rs5937843(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position74529484
GeneSLC16A2
is asnp
is mentioned by
dbSNPrs5937843
ebirs5937843
HLIrs5937843
Exacrs5937843
Varsomers5937843
Maprs5937843
PheGenIrs5937843
hapmaprs5937843
1000 genomesrs5937843
hgdprs5937843
ensemblrs5937843
gopubmedrs5937843
geneviewrs5937843
scholarrs5937843
googlers5937843
pharmgkbrs5937843
gwascentralrs5937843
openSNPrs5937843
23andMers5937843
23andMe allrs5937843
SNP Nexus

SNPshotrs5937843
SNPdbers5937843
MSV3drs5937843
GWAS Ctlgrs5937843
GMAF0.4021
Max Magnitude0
? (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,