ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.2116+1G>A

dbSNP: rs1554924540
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000666201 SCV000790454 likely pathogenic Hyperinsulinemic hypoglycemia, familial, 1 2017-03-21 criteria provided, single submitter clinical testing
Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic RCV002251499 SCV002522269 uncertain significance Maturity onset diabetes mellitus in young criteria provided, single submitter research Mutations in ABCC8 gene are associated with both neonatal diabetes mellitus as well as MODY. Patients with this mutation may have a better response to sulfonylureas. However, no sufficient evidence is found to ascertain the role of this particular variant (rs1554924540) in MODY yet.
Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic RCV002251500 SCV002522270 uncertain significance Transitory neonatal diabetes mellitus criteria provided, single submitter research Mutations in ABCC8 gene are associated with both neonatal diabetes mellitus as well as MODY. Patients with this mutation may have a better response to sulfonylureas. However, no sufficient evidence is found to ascertain the role of this particular variant (rs1554924540) in neonatal diabetes yet.

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