List of variants in gene combination LOC129931894, SLC19A2 reported as pathogenic for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006996.3(SLC19A2):c.152C>T (p.Pro51Leu)	rs121908540	0.00001
NM_006996.3(SLC19A2):c.64_70del (p.Thr22fs)	rs1557894839

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