List of variants in gene POMP 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
NC_000013.11:g.28659090del	rs112368783
NM_015932.6(POMP):c.334_335del (p.Ile112fs)	rs1555257073
NM_015932.6(POMP):c.340_344dup (p.Glu115fs)	rs1555257075
NM_015932.6(POMP):c.342_348delinsACC (p.Phe114fs)	rs1555257076

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