List of variants in gene combination STX16, STX16-NPEPL1 reported as uncertain significance for autosomal dominant pseudohypoaldosteronism type 1

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001001433.3(STX16):c.2347_2348insAAA	rs761666161
NM_001001433.3(STX16):c.*2348del	rs886056863
NM_001001433.3(STX16):c.2363_2366dup	rs10695175
NM_001001433.3(STX16):c.2364_2366dup	rs10695175
NM_001001433.3(STX16):c.*2496del	rs886056865

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