List of variants in gene RNF113A reported as pathogenic for hereditary epidermal appendage anomaly

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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_006978.3(RNF113A):c.897_898del (p.Cys299_Asp300delinsTer)	rs2056406264
NM_006978.3(RNF113A):c.901C>T (p.Gln301Ter)	rs794726863
NM_006978.3(RNF113A):c.903_910del (p.Gln302fs)	rs1603374549

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