Submissions for variant NM_017875.4(SLC25A38):c.-209A>G

gnomAD frequency: 0.01332  dbSNP: rs143903497

Total submissions: 3

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Illumina Laboratory Services, Illumina	RCV000391659	SCV000444259	benign	Sideroblastic anemia 2	2018-01-13	criteria provided, single submitter	clinical testing	This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score and internal cut-off values, a variant classified as benign is not then subjected to further curation. The score for this variant resulted in a classification of benign for this disease.
Illumina Laboratory Services, Illumina	RCV000309157	SCV000444260	likely benign	Refractory anemia with ringed sideroblasts (clinical)	2016-06-14	criteria provided, single submitter	clinical testing
GeneDx	RCV001537121	SCV001753954	likely benign	not provided	2018-06-28	criteria provided, single submitter	clinical testing