List of variants in gene GFAP reported as likely pathogenic for not provided

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_002055.5(GFAP):c.1154C>G (p.Ser385Cys)	rs797044590	0.00001
NM_002055.5(GFAP):c.1034A>C (p.His345Pro)
NM_002055.5(GFAP):c.1171+472G>A	rs748860341
NM_002055.5(GFAP):c.1220A>T (p.Asn407Ile)	rs1555573462
NM_002055.5(GFAP):c.1240del (p.Glu414fs)	rs2051680751
NM_002055.5(GFAP):c.1245G>A (p.Met415Ile)
NM_002055.5(GFAP):c.197G>A (p.Arg66Gln)	rs797044569
NM_002055.5(GFAP):c.197G>C (p.Arg66Pro)	rs797044569
NM_002055.5(GFAP):c.205G>A (p.Glu69Lys)	rs797044570
NM_002055.5(GFAP):c.209G>A (p.Arg70Gln)	rs267607510
NM_002055.5(GFAP):c.219G>A (p.Met73Ile)
NM_002055.5(GFAP):c.252C>G (p.Ile84Met)	rs571151302
NM_002055.5(GFAP):c.620A>T (p.Glu207Val)	rs1555574517
NM_002055.5(GFAP):c.708_710del (p.Glu237del)

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