ClinVar Miner

List of variants in gene GFAP reported as likely benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002055.5(GFAP):c.140C>T (p.Pro47Leu)	rs57474185	0.00543
NM_002055.5(GFAP):c.329C>G (p.Thr110Ser)	rs147282497	0.00020

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