List of variants in gene combination GFAP, LOC130060994 reported as uncertain significance by Labcorp Genetics (formerly Invitae), Labcorp

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002055.5(GFAP):c.1087A>T (p.Ile363Phe)	rs2145632673
NM_002055.5(GFAP):c.1089C>G (p.Ile363Met)	rs2508933424
NM_002055.5(GFAP):c.1111G>A (p.Glu371Lys)	rs267607526
NM_002055.5(GFAP):c.1127G>A (p.Arg376Gln)	rs2508933141

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