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rs121918702

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918702(G;G)
Make rs121918702(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position24122894
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918702
ebirs121918702
HLIrs121918702
Exacrs121918702
Varsomers121918702
Maprs121918702
PheGenIrs121918702
hapmaprs121918702
1000 genomesrs121918702
hgdprs121918702
ensemblrs121918702
gopubmedrs121918702
geneviewrs121918702
scholarrs121918702
googlers121918702
pharmgkbrs121918702
gwascentralrs121918702
openSNPrs121918702
23andMers121918702
23andMe allrs121918702
SNP Nexus

SNPshotrs121918702
SNPdbers121918702
MSV3drs121918702
GWAS Ctlgrs121918702
Max Magnitude0
OMIM190160
Desc
Variant0032
Relatedalso
ClinVar
Risk rs121918702(G;G)
Alt rs121918702(G;G)
Reference rs121918702(T;T)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, generalized
Reversed 1
HGVS NC_000003.11:g.24164385A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013389.23,