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rs121918686

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Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918686(C;C)
Make rs121918686(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position24127610
GeneTHRB
is asnp
is mentioned by
dbSNPrs121918686
ebirs121918686
HLIrs121918686
Exacrs121918686
Varsomers121918686
Maprs121918686
PheGenIrs121918686
hapmaprs121918686
1000 genomesrs121918686
hgdprs121918686
ensemblrs121918686
gopubmedrs121918686
geneviewrs121918686
scholarrs121918686
googlers121918686
pharmgkbrs121918686
gwascentralrs121918686
openSNPrs121918686
23andMers121918686
23andMe allrs121918686
SNP Nexus

SNPshotrs121918686
SNPdbers121918686
MSV3drs121918686
GWAS Ctlgrs121918686
Max Magnitude0
OMIM190160
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121918686(A,C;A,C)
Alt rs121918686(A,C;A,C)
Reference rs121918686(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.24169101C>G; NC_000003.11:g.24169101C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013362.22, RCV000013379.24,