List of variants in gene SLC39A7 reported as pathogenic for immune system disorder

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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_006979.3(SLC39A7):c.1114C>T (p.Gln372Ter)	rs201790479	0.00002
NM_006979.3(SLC39A7):c.568C>G (p.Pro190Ala)	rs563866464	0.00002
NM_006979.3(SLC39A7):c.1087G>A (p.Glu363Lys)	rs771311186	0.00001
NM_006979.3(SLC39A7):c.1184C>T (p.Thr395Ile)	rs1416107120	0.00001
NM_006979.3(SLC39A7):c.650T>C (p.Leu217Pro)	rs1170038377

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