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rs121918698

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918698(A;A)
Make rs121918698(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position24122957
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918698
ebirs121918698
HLIrs121918698
Exacrs121918698
Varsomers121918698
Maprs121918698
PheGenIrs121918698
hapmaprs121918698
1000 genomesrs121918698
hgdprs121918698
ensemblrs121918698
gopubmedrs121918698
geneviewrs121918698
scholarrs121918698
googlers121918698
pharmgkbrs121918698
gwascentralrs121918698
openSNPrs121918698
23andMers121918698
23andMe allrs121918698
SNP Nexus

SNPshotrs121918698
SNPdbers121918698
MSV3drs121918698
GWAS Ctlgrs121918698
Max Magnitude0
OMIM190160
Desc
Variant0024
Relatedalso
ClinVar
Risk rs121918698(A;A)
Alt rs121918698(A;A)
Reference rs121918698(G;G)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, generalized, autosomal dominant
Reversed 1
HGVS NC_000003.11:g.24164448C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013387.23,