List of variants in gene PRDM16 reported as uncertain significance for PRDM16-related condition

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_022114.4(PRDM16):c.490G>A (p.Gly164Arg)	rs770235387	0.00004
NM_022114.4(PRDM16):c.1484C>T (p.Pro495Leu)	rs779190595	0.00001
NM_022114.4(PRDM16):c.1877A>T (p.Asp626Val)	rs876657958	0.00001
NM_022114.4(PRDM16):c.2384C>T (p.Pro795Leu)
NM_022114.4(PRDM16):c.535G>A (p.Asp179Asn)	rs929298724
NM_022114.4(PRDM16):c.787G>A (p.Gly263Ser)	rs1478144781

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