ClinVar Miner

List of variants in gene PRMT9 reported as uncertain significance by Laboratory of Medical Genetics (UMR_S 1112), INSERM/Strasbourg University

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_138364.4(PRMT9):c.1144C>A (p.Gln382Lys)
NM_138364.4(PRMT9):c.1772T>C (p.Phe591Ser)
NM_138364.4(PRMT9):c.2405C>T (p.Thr802Ile)

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