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rs121918705

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918705(A;A)
Make rs121918705(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position24122968
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918705
ebirs121918705
HLIrs121918705
Exacrs121918705
Varsomers121918705
Maprs121918705
PheGenIrs121918705
hapmaprs121918705
1000 genomesrs121918705
hgdprs121918705
ensemblrs121918705
gopubmedrs121918705
geneviewrs121918705
scholarrs121918705
googlers121918705
pharmgkbrs121918705
gwascentralrs121918705
openSNPrs121918705
23andMers121918705
23andMe allrs121918705
SNP Nexus

SNPshotrs121918705
SNPdbers121918705
MSV3drs121918705
GWAS Ctlgrs121918705
Max Magnitude0
OMIM190160
Desc
Variant0036
Relatedalso
ClinVar
Risk rs121918705(A;A)
Alt rs121918705(A;A)
Reference rs121918705(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.24164459G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013393.16,