ClinVar Miner

List of variants in gene INSR reported as uncertain significance for Hyperinsulinism due to INSR deficiency; Leprechaunism syndrome; Rabson-Mendenhall syndrome

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)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000208.4(INSR):c.2107G>A (p.Glu703Lys)
NM_000208.4(INSR):c.2716G>A (p.Ala906Thr)
NM_000208.4(INSR):c.640C>A (p.His214Asn)

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