List of variants in gene combination LOC129996783, ZNF292 reported as uncertain significance for Inborn genetic diseases

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_015021.3(ZNF292):c.47G>C (p.Gly16Ala)	rs554384428	0.00004
NM_015021.3(ZNF292):c.40G>A (p.Gly14Ser)	rs749712579	0.00002
NM_015021.3(ZNF292):c.4G>A (p.Ala2Thr)

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