List of variants in gene LOC126860775, PRDM12 studied for Inborn genetic diseases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_021619.3(PRDM12):c.341T>C (p.Met114Thr)	rs2490723773	0.00002
NM_021619.3(PRDM12):c.391A>G (p.Lys131Glu)	rs1184031990	0.00001
NM_021619.3(PRDM12):c.271G>A (p.Ala91Thr)	rs2490723519
NM_021619.3(PRDM12):c.371C>A (p.Pro124Gln)	rs764884666

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