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rs121918690

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918690(A;A)
Make rs121918690(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position24127694
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918690
ebirs121918690
HLIrs121918690
Exacrs121918690
Varsomers121918690
Maprs121918690
PheGenIrs121918690
hapmaprs121918690
1000 genomesrs121918690
hgdprs121918690
ensemblrs121918690
gopubmedrs121918690
geneviewrs121918690
scholarrs121918690
googlers121918690
pharmgkbrs121918690
gwascentralrs121918690
openSNPrs121918690
23andMers121918690
23andMe allrs121918690
SNP Nexus

SNPshotrs121918690
SNPdbers121918690
MSV3drs121918690
GWAS Ctlgrs121918690
Max Magnitude0
OMIM190160
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121918690(A;A)
Alt rs121918690(A;A)
Reference rs121918690(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.24169185C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013369.22,