List of variants in gene GFAP reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_002055.5(GFAP):c.329C>G (p.Thr110Ser)	rs147282497	0.00020
NM_002055.5(GFAP):c.625C>T (p.Arg209Trp)	rs146725018	0.00006
NM_002055.5(GFAP):c.1036_1064del (p.Leu346fs)	rs765762750	0.00002
NM_002055.5(GFAP):c.314G>A (p.Arg105Gln)	rs751356359	0.00001
NM_002055.5(GFAP):c.406C>T (p.Arg136Trp)	rs774799414	0.00001
NM_002055.5(GFAP):c.462-8dup	rs572562362
NM_002055.5(GFAP):c.694A>G (p.Thr232Ala)	rs1182170998

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