List of variants in gene SLC39A14 reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001128431.4(SLC39A14):c.508C>G (p.Leu170Val)	rs376221087	0.00008
NM_001128431.4(SLC39A14):c.275T>A (p.Phe92Tyr)	rs201522442	0.00002
NM_001128431.4(SLC39A14):c.523G>A (p.Val175Met)
NM_001128431.4(SLC39A14):c.58G>A (p.Gly20Ser)	rs183988980
NM_001128431.4(SLC39A14):c.939+1G>A

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