ClinVar Miner

List of variants in gene THRB studied for thyroid hormone resistance, generalized, autosomal recessive

Included ClinVar conditions (2):
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Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_001354712.2(THRB):c.175A>G (p.Ile59Val) rs141172732 0.00003
NG_009159.1:g.(?_270821)_(382671_?)del
NM_001354712.2(THRB):c.1010_1012del (p.Thr337del) rs387906515
NM_001354712.2(THRB):c.1012C>T (p.Arg338Trp) rs121918697
NM_001354712.2(THRB):c.803C>A (p.Ala268Asp)
NM_001354712.2(THRB):c.803C>G (p.Ala268Gly) rs750905761
NM_001354712.2(THRB):c.958C>T (p.Arg320Cys) rs121918696

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