ClinVar Miner

Submissions for variant NM_000352.6(ABCC8):c.691T>C (p.Trp231Arg)

dbSNP: rs1554942704
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000666524 SCV000790829 uncertain significance Hyperinsulinemic hypoglycemia, familial, 1 2017-04-11 criteria provided, single submitter clinical testing
Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic RCV002253548 SCV002522654 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 (rs1554942704) in MODY yet.
Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic RCV002253549 SCV002522657 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 (rs1554942704) in neonatal diabetes yet.

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