List of variants in gene SLC39A13 reported as likely benign for not specified

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001128225.3(SLC39A13):c.-33G>C	rs538845170	0.00136
NM_001128225.3(SLC39A13):c.621C>T (p.Leu207=)	rs775396957	0.00008
NM_001128225.3(SLC39A13):c.786+8C>T	rs572017658	0.00006
NM_001128225.3(SLC39A13):c.736-18C>T	rs761758087	0.00003
NM_001128225.3(SLC39A13):c.795C>T (p.Asp265=)	rs762829962	0.00002
NM_001128225.3(SLC39A13):c.1059G>T (p.Leu353=)	rs1057524263	0.00001
NM_001128225.3(SLC39A13):c.*19C>T	rs750637189
NM_001128225.3(SLC39A13):c.-32G>T	rs552060646
NM_001128225.3(SLC39A13):c.-8-16C>A	rs1555134520
NM_001128225.3(SLC39A13):c.-8-18G>T	rs1555134508
NM_001128225.3(SLC39A13):c.153G>A (p.Lys51=)	rs529299524
NM_001128225.3(SLC39A13):c.270C>T (p.Pro90=)	rs1291377563
NM_001128225.3(SLC39A13):c.416-36TGGCC[2]	rs763461494
NM_001128225.3(SLC39A13):c.681C>T (p.Ile227=)	rs768663803
NM_001128225.3(SLC39A13):c.919+19dup	rs747836551

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