List of variants in gene SLC19A2 reported as pathogenic by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006996.3(SLC19A2):c.1082G>A (p.Trp361Ter)	rs1553211899
NM_006996.3(SLC19A2):c.428C>T (p.Ser143Phe)	rs761957186
NM_006996.3(SLC19A2):c.584_585del (p.Leu195fs)	rs763099442

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