List of variants in gene PRDM16 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_022114.4(PRDM16):c.1113C>T (p.Cys371=)	rs61745281	0.02560
NM_022114.4(PRDM16):c.627C>T (p.His209=)	rs12058363	0.02126
NM_022114.4(PRDM16):c.2793C>T (p.Asn931=)	rs59135929	0.01493
NM_022114.4(PRDM16):c.2940-17G>A	rs41301967	0.01452
NM_022114.4(PRDM16):c.783C>T (p.Tyr261=)	rs61756439	0.00952
NM_022114.4(PRDM16):c.3109+10G>A	rs7549401	0.00898
NM_022114.4(PRDM16):c.38-15C>T	rs9662053	0.00658
NM_022114.4(PRDM16):c.3369C>T (p.Asp1123=)	rs370420046	0.00537
NM_022114.4(PRDM16):c.1212G>A (p.Thr404=)	rs139129844	0.00438
NM_022114.4(PRDM16):c.387+6C>T	rs369010644	0.00373
NM_022114.4(PRDM16):c.3102C>T (p.Asn1034=)	rs199853370	0.00144
NM_022114.4(PRDM16):c.3687T>C (p.Ala1229=)	rs188634763	0.00137

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