List of variants in gene SLC39A13 reported as uncertain significance for autoimmune disease

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_001128225.3(SLC39A13):c.398C>T (p.Thr133Met)	rs140574574

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