Submissions for variant NM_000208.4(INSR):c.653-23TC[11]

dbSNP: rs3835070

Total submissions: 10

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Genetic Services Laboratory, University of Chicago	RCV000194846	SCV000247623	benign	not specified	2014-11-18	criteria provided, single submitter	clinical testing
Illumina Laboratory Services, Illumina	RCV000363699	SCV000415568	benign	Rabson-Mendenhall syndrome	2016-06-14	criteria provided, single submitter	clinical testing
Illumina Laboratory Services, Illumina	RCV000271370	SCV000415569	benign	Leprechaunism syndrome	2016-06-14	criteria provided, single submitter	clinical testing
Illumina Laboratory Services, Illumina	RCV000328745	SCV000415570	benign	Insulin-resistant diabetes mellitus AND acanthosis nigricans	2016-06-14	criteria provided, single submitter	clinical testing
Eurofins Ntd Llc (ga)	RCV000194846	SCV000857741	benign	not specified	2017-10-23	criteria provided, single submitter	clinical testing
GeneDx	RCV001572815	SCV001912879	benign	not provided	2021-06-09	criteria provided, single submitter	clinical testing
Invitae	RCV001572815	SCV002341742	benign	not provided	2024-01-31	criteria provided, single submitter	clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC)	RCV001572815	SCV001797772	likely benign	not provided		no assertion criteria provided	clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht	RCV001572815	SCV001932731	likely benign	not provided		no assertion criteria provided	clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center	RCV000194846	SCV001975764	benign	not specified		no assertion criteria provided	clinical testing