"GeneDx"[submitter] AND "ZSCAN29"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1228847	NM_001372080.1(ZSCAN29):c.2508C>T (p.His836=)	ZSCAN29	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1188532	NC_000015.10:g.43370961G>C	LOC130056943, TUBGCP4 +1 more	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign
Select item 1242749	NC_000015.10:g.43370977CCCGGC[7]	LOC130056943, TUBGCP4 +1 more	Microsatellite (5 prime UTR variant)	not provided	GBenign
Select item 1237521	NC_000015.10:g.43370977CCCGGC[6]	LOC130056943, TUBGCP4 +1 more	Microsatellite (5 prime UTR variant)	not provided	GBenign
Select item 1208069	NC_000015.10:g.43370977CCCGGC[10]	LOC130056943, TUBGCP4 +1 more	Microsatellite (5 prime UTR variant)	not provided	GLikely benign
Select item 1197063	NC_000015.10:g.43370977CCCGGC[9]	LOC130056943, TUBGCP4 +1 more	Microsatellite (5 prime UTR variant)	not provided	GLikely benign
Select item 1240667	NC_000015.10:g.43370977CCCGGC[4]	LOC130056943, TUBGCP4 +1 more	Microsatellite (5 prime UTR variant)	not provided	GBenign
Select item 1196047	NC_000015.10:g.43371012A>G	TUBGCP4, ZSCAN29	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign

ClinVar