List of variants in gene LOC129931894, SLC19A2 studied for hematologic disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_006996.3(SLC19A2):c.-2G>A	rs886045531	0.00006
NM_006996.3(SLC19A2):c.10C>T (p.Pro4Ser)	rs886045530	0.00006
NM_006996.3(SLC19A2):c.30G>A (p.Arg10=)	rs928593954	0.00002
NM_006996.3(SLC19A2):c.42G>T (p.Ala14=)	rs945252214	0.00002
NM_006996.3(SLC19A2):c.104C>T (p.Ala35Val)	rs756487822	0.00001
NM_006996.3(SLC19A2):c.124T>G (p.Phe42Val)	rs1490832268	0.00001
NM_006996.3(SLC19A2):c.152C>T (p.Pro51Leu)	rs121908540	0.00001
NM_006996.3(SLC19A2):c.30GGC[5] (p.Ala16del)
NM_006996.3(SLC19A2):c.64_70del (p.Thr22fs)	rs1557894839

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