List of variants in gene GFAP reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002055.5(GFAP):c.621G>T (p.Glu207Asp)	rs759844035
NM_002055.5(GFAP):c.646G>A (p.Ala216Thr)
NM_002055.5(GFAP):c.715C>T (p.Arg239Cys)	rs58064122
NM_002055.5(GFAP):c.716G>A (p.Arg239His)	rs59565950
NM_002055.5(GFAP):c.909C>G (p.Asn303Lys)

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