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rs121918704

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918704(C;C)
Make rs121918704(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position24122897
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918704
ebirs121918704
HLIrs121918704
Exacrs121918704
Varsomers121918704
Maprs121918704
PheGenIrs121918704
hapmaprs121918704
1000 genomesrs121918704
hgdprs121918704
ensemblrs121918704
gopubmedrs121918704
geneviewrs121918704
scholarrs121918704
googlers121918704
pharmgkbrs121918704
gwascentralrs121918704
openSNPrs121918704
23andMers121918704
23andMe allrs121918704
SNP Nexus

SNPshotrs121918704
SNPdbers121918704
MSV3drs121918704
GWAS Ctlgrs121918704
Max Magnitude0
OMIM190160
Desc
Variant0035
Relatedalso
ClinVar
Risk rs121918704(C;C)
Alt rs121918704(C;C)
Reference rs121918704(T;T)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, generalized, autosomal recessive
Reversed 1
HGVS NC_000003.11:g.24164388A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013392.24,