List of variants in gene TBL1X 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_005647.4(TBL1X):c.1015C>T (p.Arg339Ter)	rs1601844140
NM_005647.4(TBL1X):c.1246A>T (p.Asn416Tyr)	rs1601855785
NM_005647.4(TBL1X):c.1510C>T (p.His504Tyr)	rs1601857538
NM_005647.4(TBL1X):c.1526A>G (p.Tyr509Cys)	rs1601857555

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