List of variants in gene GFAP reported as pathogenic by Illumina Laboratory Services, Illumina

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_002055.5(GFAP):c.235C>T (p.Arg79Cys)	rs59793293	0.00001
NM_002055.5(GFAP):c.259G>C (p.Val87Leu)	rs267607518
NM_002055.5(GFAP):c.715C>T (p.Arg239Cys)	rs58064122

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