List of variants in gene INSR reported as pathogenic for not provided

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000208.4(INSR):c.1246C>T (p.Arg416Ter)	rs778989302	0.00001
NM_000208.4(INSR):c.1348C>T (p.Gln450Ter)	rs2144950571
NM_000208.4(INSR):c.2164G>T (p.Glu722Ter)
NM_000208.4(INSR):c.25dup (p.Ala9fs)
NM_000208.4(INSR):c.350_353del (p.Asn117fs)	rs1347163319
NM_000208.4(INSR):c.3602G>A (p.Arg1201Gln)	rs121913156
NM_000208.4(INSR):c.3633_3634del (p.Val1212fs)
NM_000208.4(INSR):c.509dup (p.Asn170fs)

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