Variants in gene ZNF142 with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_001379659.1(ZNF142):c.5098C>T (p.Arg1700Trp)	rs367658234	0.00003
NM_001379659.1(ZNF142):c.4298G>T (p.Cys1433Phe)	rs1275959058	0.00001
NM_001379659.1(ZNF142):c.916C>T (p.Gln306Ter)	rs2469743343

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