List of variants in gene WRAP53 reported as likely pathogenic for ectodermal dysplasia syndrome

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001143992.2(WRAP53):c.1192C>T (p.Arg398Trp)	rs281865548	0.00016
NM_001143992.2(WRAP53):c.1257del (p.Phe419fs)
NM_001143992.2(WRAP53):c.438G>A (p.Trp146Ter)
NM_001143992.2(WRAP53):c.509del (p.Asn170fs)

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