List of variants in gene IVNS1ABP reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006469.5(IVNS1ABP):c.1399A>G (p.Ile467Val)	rs781116659	0.00002
NM_006469.5(IVNS1ABP):c.1642G>T (p.Ala548Ser)
NM_006469.5(IVNS1ABP):c.1675G>C (p.Gly559Arg)	rs1460740417
NM_006469.5(IVNS1ABP):c.379T>C (p.Ser127Pro)	rs959035894
NM_006469.5(IVNS1ABP):c.878C>T (p.Ala293Val)
NM_006469.5(IVNS1ABP):c.934T>C (p.Phe312Leu)	rs375500212

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