List of variants in gene DPP6 reported as uncertain significance by Mendelics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_130797.4(DPP6):c.627+21101A>G	rs117574002	0.00365
NM_130797.4(DPP6):c.2304G>C (p.Glu768Asp)	rs1584993945	0.00001
NM_130797.4(DPP6):c.2304+2T>C	rs931703283

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