List of variants in gene PRDM16 reported as likely pathogenic for not provided

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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
GRCh37/hg19 1p36.32(chr1:3101762-3155604)x1
NM_022114.4(PRDM16):c.1459del (p.Glu487fs)	rs1085307663
NM_022114.4(PRDM16):c.1989del (p.Glu664fs)	rs1553176765
NM_022114.4(PRDM16):c.259C>T (p.Arg87Ter)

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