List of variants in gene PRDM12 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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_021619.3(PRDM12):c.127A>G (p.Asn43Asp)	rs149449772	0.00016
NM_021619.3(PRDM12):c.440G>A (p.Arg147His)	rs139807684	0.00006
NM_021619.3(PRDM12):c.1028A>C (p.His343Pro)	rs1443107336	0.00004
NM_021619.3(PRDM12):c.503G>A (p.Arg168His)	rs1049529374
NM_021619.3(PRDM12):c.787C>A (p.Arg263Ser)
NM_021619.3(PRDM12):c.992A>G (p.Gln331Arg)

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