"PreventionGenetics, part of Exact Sciences"[submitter] AND "ZP2"[gene - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3051221	NM_001376232.1(ZP2):c.2096-5dup	ZP2	Duplication (intron variant)	ZP2-related condition	GLikely benign
Select item 3038807	NM_001376232.1(ZP2):c.1815C>T (p.His605=)	ZP2	Single nucleotide variant (synonymous variant +1 more)	ZP2-related condition	GLikely benign
Select item 3040441	NM_001376232.1(ZP2):c.1100-9G>A	ZP2	Single nucleotide variant (intron variant)	ZP2-related condition	GLikely benign
Select item 3040963	NM_001376232.1(ZP2):c.1099+9C>A	ZP2	Single nucleotide variant (intron variant)	ZP2-related condition	GLikely benign
Select item 3060177	NM_001376232.1(ZP2):c.747T>C (p.Pro249=)	ZP2	Single nucleotide variant (synonymous variant +1 more)	ZP2-related condition	GBenign
Select item 3058946	NM_001376232.1(ZP2):c.519C>T (p.Asp173=)	ZP2	Single nucleotide variant (synonymous variant +1 more)	ZP2-related condition	GBenign
Select item 710348	NM_001376232.1(ZP2):c.495A>C (p.Pro165=)	ZP2	Single nucleotide variant (synonymous variant +1 more)	ZP2-related condition +1 more	GBenign
Select item 714693	NM_001376232.1(ZP2):c.460A>G (p.Ile154Val)	ZP2 (I154V)	Single nucleotide variant (missense variant +1 more)	ZP2-related condition +1 more	GBenign
Select item 3039783	NM_001376232.1(ZP2):c.152-6C>T	ZP2	Single nucleotide variant (intron variant)	ZP2-related condition	GLikely benign
Select item 3060011	NM_001376232.1(ZP2):c.107G>T (p.Gly36Val)	ZP2 (G36V)	Single nucleotide variant (missense variant +1 more)	ZP2-related condition	GBenign
Select item 3039472	NM_001376232.1(ZP2):c.-9T>C	ZP2	Single nucleotide variant (5 prime UTR variant +1 more)	ZP2-related condition	GBenign