List of variants in gene combination GNPTG, UNKL reported as uncertain significance for GNPTAB-mucolipidosis

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_032520.5(GNPTG):c.*257dup	rs539354203	0.00242
NM_032520.5(GNPTG):c.*233C>T	rs890946572	0.00006
NM_032520.5(GNPTG):c.*165A>T	rs2034976804
NM_032520.5(GNPTG):c.*205T>C	rs886051686

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