List of variants in gene TSHB reported as pathogenic for hypothyroidism, congenital, nongoitrous

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000549.5(TSHB):c.373del (p.Cys125fs)	rs755485552	0.00017
NM_000549.5(TSHB):c.205C>T (p.Gln69Ter)	rs121918670	0.00002
NM_000549.5(TSHB):c.162+5G>A	rs868637545	0.00001
NM_000549.5(TSHB):c.108_109del (p.Ala37fs)	rs2101008674
NM_000549.5(TSHB):c.145G>A (p.Gly49Arg)	rs121918668
NM_000549.5(TSHB):c.94G>T (p.Glu32Ter)	rs121918669

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