List of variants in gene SLC39A4 reported as benign by Natera, Inc.

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_130849.4(SLC39A4):c.172G>A (p.Ala58Thr)	rs2280838	0.51612
NM_130849.4(SLC39A4):c.193-89A>C	rs2280839	0.49986
NM_130849.4(SLC39A4):c.340G>A (p.Ala114Thr)	rs17855765	0.43910
NM_130849.4(SLC39A4):c.1069A>G (p.Thr357Ala)	rs2272662	0.43646
NM_130849.4(SLC39A4):c.193-113T>C	rs115637224	0.05521
NM_130849.4(SLC39A4):c.1141A>G (p.Thr381Ala)	rs75920625	0.04681
NM_130849.4(SLC39A4):c.63G>C (p.Thr21=)	rs13251676	0.04058
NM_130849.4(SLC39A4):c.850G>A (p.Glu284Lys)	rs7823979	0.02971
NM_130849.4(SLC39A4):c.251C>T (p.Pro84Leu)	rs117535951	0.02765
NM_130849.4(SLC39A4):c.276C>T (p.Tyr92=)	rs4355816	0.02200
NM_130849.4(SLC39A4):c.948C>T (p.Pro316=)	rs60615103	0.00469
NM_130849.4(SLC39A4):c.532A>T (p.Ser178Cys)	rs113717209	0.00402
NM_130849.4(SLC39A4):c.1495A>G (p.Met499Val)	rs145832695	0.00335
NM_130849.4(SLC39A4):c.10C>T (p.Leu4=)	rs144946747	0.00288
NM_130849.4(SLC39A4):c.1659G>C (p.Leu553=)	rs143778004	0.00170
NM_130849.4(SLC39A4):c.595T>C (p.Leu199=)	rs141199511	0.00155
NM_130849.4(SLC39A4):c.257C>T (p.Pro86Leu)	rs187080747	0.00098
NM_130849.4(SLC39A4):c.390C>T (p.Leu130=)	rs782454483	0.00039
NM_130849.4(SLC39A4):c.1126G>A (p.Ala376Thr)	rs200073988	0.00024
NM_130849.4(SLC39A4):c.1204C>T (p.Arg402Cys)	rs199542349	0.00016
NM_130849.4(SLC39A4):c.646G>A (p.Glu216Lys)	rs200524049	0.00009
NM_130849.4(SLC39A4):c.213C>T (p.Ala71=)	rs577104686	0.00006
NM_130849.4(SLC39A4):c.225C>T (p.Gly75=)	rs376105192	0.00003

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