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rs121918701

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918701(A;A)
Make rs121918701(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position24122921
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918701
ebirs121918701
HLIrs121918701
Exacrs121918701
Varsomers121918701
Maprs121918701
PheGenIrs121918701
hapmaprs121918701
1000 genomesrs121918701
hgdprs121918701
ensemblrs121918701
gopubmedrs121918701
geneviewrs121918701
scholarrs121918701
googlers121918701
pharmgkbrs121918701
gwascentralrs121918701
openSNPrs121918701
23andMers121918701
23andMe allrs121918701
SNP Nexus

SNPshotrs121918701
SNPdbers121918701
MSV3drs121918701
GWAS Ctlgrs121918701
Max Magnitude0
OMIM190160
Desc
Variant0030
Relatedalso
ClinVar
Risk rs121918701(A;A)
Alt rs121918701(A;A)
Reference rs121918701(T;T)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, generalized
Reversed 1
HGVS NC_000003.11:g.24164412A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013375.24,