List of variants in gene INSR reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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_000208.4(INSR):c.2843-5T>G	rs1555736265
NM_000208.4(INSR):c.3470A>G (p.His1157Arg)	rs957304581
NM_000208.4(INSR):c.3668G>A (p.Gly1223Asp)	rs1555734564
NM_000208.4(INSR):c.421C>T (p.Arg141Trp)	rs1555689823
NM_000208.4(INSR):c.728G>A (p.Cys243Tyr)	rs911809758

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