List of variants in gene SLC30A2 reported as uncertain significance

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_001004434.3(SLC30A2):c.988G>A (p.Ala330Thr)	rs149723161	0.00029
NM_001004434.3(SLC30A2):c.215G>A (p.Arg72His)	rs368255248	0.00003
NM_001004434.3(SLC30A2):c.927G>C (p.Trp309Cys)	rs1185652351	0.00003
NM_001004434.3(SLC30A2):c.11A>G (p.Lys4Arg)	rs1383240690	0.00001
NM_001004434.3(SLC30A2):c.945G>C (p.Gln315His)	rs1233216949	0.00001
NM_001004434.3(SLC30A2):c.1001T>C (p.Leu334Pro)	rs2522673106
NM_001004434.3(SLC30A2):c.1018C>G (p.Arg340Gly)	rs35623192
NM_001004434.3(SLC30A2):c.1106G>A (p.Gly369Asp)	rs2124419907
NM_001004434.3(SLC30A2):c.127A>G (p.Ile43Val)	rs2522698577
NM_001004434.3(SLC30A2):c.146G>A (p.Ser49Asn)	rs2522698482
NM_001004434.3(SLC30A2):c.280C>G (p.Leu94Val)
NM_001004434.3(SLC30A2):c.281T>C (p.Leu94Pro)
NM_001004434.3(SLC30A2):c.310G>C (p.Ala104Pro)
NM_001004434.3(SLC30A2):c.573A>G (p.Ile191Met)	rs1219015034
NM_001004434.3(SLC30A2):c.577G>C (p.Gly193Arg)
NM_001004434.3(SLC30A2):c.616G>A (p.Gly206Ser)	rs760380190
NM_001004434.3(SLC30A2):c.637G>C (p.Glu213Gln)
NM_001004434.3(SLC30A2):c.649G>A (p.Val217Ile)
NM_001004434.3(SLC30A2):c.649G>C (p.Val217Leu)	rs373747848
NM_001004434.3(SLC30A2):c.655G>A (p.Ala219Thr)	rs864622019
NM_001004434.3(SLC30A2):c.76G>A (p.Glu26Lys)	rs2522698871
NM_001004434.3(SLC30A2):c.80G>A (p.Gly27Glu)
NM_001004434.3(SLC30A2):c.853G>A (p.Val285Ile)
NM_001004434.3(SLC30A2):c.868G>A (p.Val290Ile)
NM_001004434.3(SLC30A2):c.917T>C (p.Leu306Pro)

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