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

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 8

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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.3775C>T (p.Arg1259Ter)	rs546151500	0.00002
NM_001379659.1(ZNF142):c.1765_1766del (p.Asp589fs)	rs750681891	0.00001
NM_001379659.1(ZNF142):c.4298G>T (p.Cys1433Phe)	rs1275959058	0.00001
NM_001105537.3(ZNF142):c.[4183delC;4185G>A]
NM_001379659.1(ZNF142):c.1417_1418del (p.Lys473fs)	rs1447313633
NM_001379659.1(ZNF142):c.1892del (p.Cys631fs)	rs1559296368
NM_001379659.1(ZNF142):c.2510del (p.Pro837fs)	rs34864794

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