List of variants in gene SLC39A13 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001128225.3(SLC39A13):c.439C>G (p.Gln147Glu)	rs148291843	0.00217
NM_001128225.3(SLC39A13):c.216C>T (p.Leu72=)	rs34986695	0.00211
NM_001128225.3(SLC39A13):c.948G>A (p.Thr316=)	rs531462966	0.00007
NM_001128225.3(SLC39A13):c.816C>T (p.Ala272=)	rs764438635	0.00001
NM_001128225.3(SLC39A13):c.879C>T (p.Gly293=)	rs1047022550	0.00001
NM_001128225.3(SLC39A13):c.398C>T (p.Thr133Met)	rs140574574
NM_001128225.3(SLC39A13):c.492G>T (p.Ala164=)	rs149634596
NM_001128225.3(SLC39A13):c.735+362G>A

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