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rs121918699

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121918699(C;C)
Make rs121918699(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position24127714
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918699
ebirs121918699
HLIrs121918699
Exacrs121918699
Varsomers121918699
Maprs121918699
PheGenIrs121918699
hapmaprs121918699
1000 genomesrs121918699
hgdprs121918699
ensemblrs121918699
gopubmedrs121918699
geneviewrs121918699
scholarrs121918699
googlers121918699
pharmgkbrs121918699
gwascentralrs121918699
openSNPrs121918699
23andMers121918699
23andMe allrs121918699
SNP Nexus

SNPshotrs121918699
SNPdbers121918699
MSV3drs121918699
GWAS Ctlgrs121918699
Max Magnitude0
OMIM190160
Desc
Variant0026
Relatedalso
ClinVar
Risk rs121918699(C;C)
Alt rs121918699(C;C)
Reference rs121918699(T;T)
Significance Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, generalized
Reversed 1
HGVS NC_000003.11:g.24169205A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013367.23,