List of variants in gene ZNF292 reported as uncertain significance by Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_015021.3(ZNF292):c.2632A>G (p.Ile878Val)	rs1256311307	0.00002
NM_015021.3(ZNF292):c.1034G>C (p.Gly345Ala)	rs2482283134
NM_015021.3(ZNF292):c.1388A>C (p.Glu463Ala)	rs1775133764
NM_015021.3(ZNF292):c.2059T>A (p.Phe687Ile)	rs200991861
NM_015021.3(ZNF292):c.3260C>T (p.Pro1087Leu)	rs1775252925
NM_015021.3(ZNF292):c.4300T>A (p.Leu1434Met)	rs2482325784
NM_015021.3(ZNF292):c.5083A>C (p.Asn1695His)	rs2482337555
NM_015021.3(ZNF292):c.6268G>C (p.Glu2090Gln)
NM_015021.3(ZNF292):c.7021T>A (p.Leu2341Ile)	rs1270393952

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