List of variants in gene ZNF292 reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_015021.3(ZNF292):c.4825A>G (p.Ile1609Val)	rs201381838	0.00001
NM_015021.3(ZNF292):c.2053G>A (p.Val685Ile)
NM_015021.3(ZNF292):c.406G>A (p.Ala136Thr)	rs2482036069
NM_015021.3(ZNF292):c.4895A>G (p.Lys1632Arg)	rs751433789
NM_015021.3(ZNF292):c.5591A>G (p.Asn1864Ser)	rs2482345316
NM_015021.3(ZNF292):c.5640C>G (p.Ile1880Met)	rs2482346053
NM_015021.3(ZNF292):c.5920T>C (p.Phe1974Leu)
NM_015021.3(ZNF292):c.6424G>C (p.Asp2142His)
NM_015021.3(ZNF292):c.7219T>C (p.Tyr2407His)	rs2482368091

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