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rs121918691

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918691(A;G)
Make rs121918691(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position24122946
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918691
ebirs121918691
HLIrs121918691
Exacrs121918691
Varsomers121918691
Maprs121918691
PheGenIrs121918691
hapmaprs121918691
1000 genomesrs121918691
hgdprs121918691
ensemblrs121918691
gopubmedrs121918691
geneviewrs121918691
scholarrs121918691
googlers121918691
pharmgkbrs121918691
gwascentralrs121918691
openSNPrs121918691
23andMers121918691
23andMe allrs121918691
SNP Nexus

SNPshotrs121918691
SNPdbers121918691
MSV3drs121918691
GWAS Ctlgrs121918691
Max Magnitude0
OMIM190160
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121918691(G;G)
Alt rs121918691(G;G)
Reference rs121918691(A;A)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, generalized, autosomal dominant
Reversed 1
HGVS NC_000003.11:g.24164437T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013374.16,