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rs121918706

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918706(A;A)
Make rs121918706(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position24143511
GeneLOC101927854, THRB
is asnp
is mentioned by
dbSNPrs121918706
ebirs121918706
HLIrs121918706
Exacrs121918706
Varsomers121918706
Maprs121918706
PheGenIrs121918706
hapmaprs121918706
1000 genomesrs121918706
hgdprs121918706
ensemblrs121918706
gopubmedrs121918706
geneviewrs121918706
scholarrs121918706
googlers121918706
pharmgkbrs121918706
gwascentralrs121918706
openSNPrs121918706
23andMers121918706
23andMe allrs121918706
SNP Nexus

SNPshotrs121918706
SNPdbers121918706
MSV3drs121918706
GWAS Ctlgrs121918706
Max Magnitude0
OMIM190160
Desc
Variant0037
Relatedalso
ClinVar
Risk rs121918706(A;A)
Alt rs121918706(A;A)
Reference rs121918706(G;G)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene LOC101927854 THRB
CLNDBN Thyroid hormone resistance, generalized, autosomal dominant
Reversed 1
HGVS NC_000003.11:g.24185002C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013394.16,