List of variants in gene THRA reported as pathogenic 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_199334.5(THRA):c.1110G>C (p.Lys370Asn)	rs137853163
NM_199334.5(THRA):c.1176C>A (p.Cys392Ter)	rs876657394
NM_199334.5(THRA):c.1193C>G (p.Pro398Arg)	rs876657396
NM_199334.5(THRA):c.1207G>A (p.Glu403Lys)	rs876657395
NM_199334.5(THRA):c.134G>T (p.Ser45Ile)	rs137853162

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