List of variants in gene IGSF1 reported as likely pathogenic for thyroid gland disorder

Minimum submission review status:		Collection method:
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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001555.5(IGSF1):c.1614G>A (p.Trp538Ter)
NM_001555.5(IGSF1):c.2042-1_2042del
NM_001555.5(IGSF1):c.2407dup (p.His803fs)	rs1603404297
NM_001555.5(IGSF1):c.3868C>T (p.Arg1290Ter)

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