List of variants in gene SLC39A13 reported as benign by GeneDx

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_001128225.3(SLC39A13):c.920-59G>T	rs11039228	0.99476
NM_001128225.3(SLC39A13):c.301+88G>C	rs755554	0.64473
NM_001128225.3(SLC39A13):c.538-174G>A	rs6485756	0.64436
NM_001128225.3(SLC39A13):c.-9+245T>C	rs7937331	0.64411
NM_001128225.3(SLC39A13):c.537+203_537+204insTACCAGGT	rs754970752	0.30807
NM_001128225.3(SLC39A13):c.537+202_537+203insGG	rs145788999	0.30757
NM_001128225.3(SLC39A13):c.301+20C>T	rs755555	0.27982
NM_001128225.3(SLC39A13):c.573G>A (p.Ala191=)	rs2293576	0.25113
NM_001128225.3(SLC39A13):c.-8-109G>A	rs753812	0.21590
NM_001128225.3(SLC39A13):c.301+15G>A	rs61000762	0.20155
NM_001128225.3(SLC39A13):c.58A>G (p.Thr20Ala)	rs61897432	0.11400
NM_001128225.3(SLC39A13):c.-8-348T>G	rs79793569	0.04583
NM_001128225.3(SLC39A13):c.-8-73G>A	rs78598727	0.03249
NM_001128225.3(SLC39A13):c.645+31G>A	rs115209143	0.03240
NM_001128225.3(SLC39A13):c.119G>A (p.Arg40Gln)	rs35741412	0.01241
NM_001128225.3(SLC39A13):c.*288C>T	rs2293577
NM_001128225.3(SLC39A13):c.-29CGC[7]	rs551004316
NM_001128225.3(SLC39A13):c.537+312dup	rs1187342398

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