Have questions? Visit https://www.reddit.com/r/SNPedia

rs121918687

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918687(A;A)
Make rs121918687(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position24122912
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918687
ebirs121918687
HLIrs121918687
Exacrs121918687
Varsomers121918687
Maprs121918687
PheGenIrs121918687
hapmaprs121918687
1000 genomesrs121918687
hgdprs121918687
ensemblrs121918687
gopubmedrs121918687
geneviewrs121918687
scholarrs121918687
googlers121918687
pharmgkbrs121918687
gwascentralrs121918687
openSNPrs121918687
23andMers121918687
23andMe allrs121918687
SNP Nexus

SNPshotrs121918687
SNPdbers121918687
MSV3drs121918687
GWAS Ctlgrs121918687
Max Magnitude0
OMIM190160
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121918687(A;A)
Alt rs121918687(A;A)
Reference rs121918687(C;C)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, generalized, autosomal dominant
Reversed 1
HGVS NC_000003.11:g.24164403G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013364.23,