List of variants in gene GNAO1 reported as not provided 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_020988.3(GNAO1):c.118G>T (p.Gly40Trp)	rs886041715
NM_020988.3(GNAO1):c.143C>T (p.Thr48Ile)	rs1555499800
NM_020988.3(GNAO1):c.625C>T (p.Arg209Cys)	rs886039494

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