List of variants reported as likely pathogenic for thyroid gland disorder by Mendelics

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000441.2(SLC26A4):c.929C>T (p.Ala310Val)	rs540008835	0.00003
NM_000441.2(SLC26A4):c.1439T>A (p.Val480Asp)	rs1314376649

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