List of variants in gene PRDM6 reported as pathogenic

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001136239.4(PRDM6):c.1385A>G (p.Gln462Arg)	rs879253872
NM_001136239.4(PRDM6):c.1646G>A (p.Arg549Gln)	rs879255278
NM_001136239.4(PRDM6):c.788G>C (p.Cys263Ser)	rs879255279

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