List of variants in gene ZNF292 reported as uncertain significance by Labcorp Genetics (formerly Invitae), Labcorp

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_015021.3(ZNF292):c.1066G>A (p.Ala356Thr)	rs976963327
NM_015021.3(ZNF292):c.2758G>C (p.Gly920Arg)	rs1775214847
NM_015021.3(ZNF292):c.3568C>G (p.Pro1190Ala)	rs1775274397
NM_015021.3(ZNF292):c.4012T>G (p.Ser1338Ala)
NM_015021.3(ZNF292):c.5939T>G (p.Val1980Gly)	rs2127870871
NM_015021.3(ZNF292):c.6175G>A (p.Val2059Met)
NM_015021.3(ZNF292):c.8152A>G (p.Thr2718Ala)	rs1775618174

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