List of variants in gene PRIMA1 reported as pathogenic for epilepsy

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: 4

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HGVS	dbSNP	gnomAD frequency
NC_000014.8:g.(?_94187790)_(94254064_?)del
NC_000014.8:g.(?_94245502)_(94245677_?)del
NM_178013.4(PRIMA1):c.270G>A (p.Trp90Ter)	rs2141161066
NM_178013.4(PRIMA1):c.80G>A (p.Trp27Ter)

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