List of variants in gene C14orf39 reported as pathogenic

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_174978.3(C14orf39):c.1180-3C>G	rs1891315296
NM_174978.3(C14orf39):c.139_142del (p.Thr47fs)
NM_174978.3(C14orf39):c.204_205del (p.His68fs)	rs1406759691
NM_174978.3(C14orf39):c.958G>T (p.Glu320Ter)	rs997282049

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