List of variants in gene PRDM16 reported as uncertain significance by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_022114.4(PRDM16):c.1093G>T (p.Ala365Ser)	rs200562747	0.00035
NM_022114.4(PRDM16):c.3406G>A (p.Gly1136Arg)	rs775245244	0.00014
NM_022114.4(PRDM16):c.1537G>A (p.Gly513Ser)	rs200278862	0.00009
NM_022114.4(PRDM16):c.2953G>A (p.Asp985Asn)	rs758565663	0.00009
NM_022114.4(PRDM16):c.115G>A (p.Glu39Lys)	rs775285788	0.00007
NM_022114.4(PRDM16):c.197C>T (p.Ser66Leu)	rs374012976	0.00007
NM_022114.4(PRDM16):c.398C>T (p.Thr133Met)	rs530119550	0.00006
NM_022114.4(PRDM16):c.2663G>A (p.Arg888Gln)	rs201119848	0.00003
NM_022114.4(PRDM16):c.1573C>T (p.Arg525Trp)	rs369644938	0.00001
NM_022114.4(PRDM16):c.215T>G (p.Val72Gly)	rs1208537671	0.00001
NM_022114.4(PRDM16):c.3281A>G (p.Lys1094Arg)	rs947863770	0.00001
NM_022114.4(PRDM16):c.1106C>A (p.Pro369His)	rs1199723250
NM_022114.4(PRDM16):c.1484C>A (p.Pro495Gln)	rs779190595
NM_022114.4(PRDM16):c.2035G>A (p.Asp679Asn)	rs772689095
NM_022114.4(PRDM16):c.2855C>A (p.Thr952Lys)	rs749180764

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