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rs6647476

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs6647476(C;C)
Make rs6647476(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position74421734
GeneSLC16A2
is asnp
is mentioned by
dbSNPrs6647476
ebirs6647476
HLIrs6647476
Exacrs6647476
Varsomers6647476
Maprs6647476
PheGenIrs6647476
hapmaprs6647476
1000 genomesrs6647476
hgdprs6647476
ensemblrs6647476
gopubmedrs6647476
geneviewrs6647476
scholarrs6647476
googlers6647476
pharmgkbrs6647476
gwascentralrs6647476
openSNPrs6647476
23andMers6647476
23andMe allrs6647476
SNP Nexus

SNPshotrs6647476
SNPdbers6647476
MSV3drs6647476
GWAS Ctlgrs6647476
GMAF0.367
Max Magnitude0

[PMID 23978482] Associations between single nucleotide polymorphisms in thyroid hormone transporter genes (MCT8, MCT10 and OATP1C1) and circulating thyroid hormones

ClinVar
Risk rs6647476(C;C)
Alt rs6647476(C;C)
Reference rs6647476(T;T)
Significance Non-pathogenic
Disease Allan-Herndon-Dudley syndrome not specified
Variation info
Gene SLC16A2
CLNDBN Allan-Herndon-Dudley syndrome not specified
Reversed 0
HGVS NC_000023.10:g.73641569T>C
CLNSRC ClinVar Emory University GeneReviews University of Chicago
CLNACC RCV000020650.1, RCV000081443.5,


[PMID 18710470] Prevalence and functional analysis of the S107P polymorphism (rs6647476) of the monocarboxylate transporter 8 (SLC16A2) gene in the male population of north-west Spain (Galicia).