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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000549.5(TSHB):c.*64T>C	rs41312672	0.00368
NM_000549.5(TSHB):c.256G>A (p.Gly86Arg)	rs190110651	0.00026
NM_000549.5(TSHB):c.374G>A (p.Cys125Tyr)	rs1430091875

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