List of variants in gene combination INSRR, NTRK1 reported as uncertain significance for Familial medullary thyroid carcinoma

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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_014215.3(INSRR):c.3319G>T (p.Ala1107Ser)	rs779943666	0.00003
NM_014215.3(INSRR):c.3537dup (p.Val1180fs)	rs761392074	0.00001
NM_014215.3(INSRR):c.3397+4del	rs1451820799
NM_014215.3(INSRR):c.3397+9G>A	rs1322273300

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