List of variants in gene SLC39A7 reported as benign for not provided

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_006979.3(SLC39A7):c.627C>G (p.Ser209=)	rs1547387	0.08405
NM_006979.3(SLC39A7):c.581-10C>A	rs41266701	0.07067
NM_006979.3(SLC39A7):c.370G>C (p.Gly124Arg)	rs35690712	0.02813
NM_006979.3(SLC39A7):c.259G>A (p.Asp87Asn)	rs34211188	0.02642
NM_006979.3(SLC39A7):c.471C>T (p.Pro157=)	rs11538810	0.00928
NM_006979.3(SLC39A7):c.160T>C (p.Phe54Leu)	rs76929655	0.00841
NM_006979.3(SLC39A7):c.744T>C (p.His248=)	rs113198103	0.00762
NM_006979.3(SLC39A7):c.171C>A (p.Gly57=)	rs2975297	0.00046
NM_006979.3(SLC39A7):c.847A>C (p.Thr283Pro)	rs200100279	0.00030
NM_006979.3(SLC39A7):c.789T>C (p.His263=)	rs34836401	0.00028
NM_006979.3(SLC39A7):c.1057A>G (p.Met353Val)	rs200791329	0.00020

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