List of variants in gene GFAP reported as uncertain significance for Inborn genetic diseases

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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.77C>T (p.Ala26Val)	rs139837765	0.00007
NM_002055.5(GFAP):c.1005del (p.Gln336fs)	rs2051758860
NM_002055.5(GFAP):c.1135A>G (p.Ile379Val)
NM_002055.5(GFAP):c.1171G>A (p.Glu391Lys)
NM_002055.5(GFAP):c.1220A>C (p.Asn407Thr)	rs1555573462
NM_002055.5(GFAP):c.13C>T (p.Arg5Cys)
NM_002055.5(GFAP):c.235del (p.Arg79fs)	rs869312938
NM_002055.5(GFAP):c.31C>G (p.Arg11Gly)
NM_002055.5(GFAP):c.325C>A (p.Pro109Thr)
NM_002055.5(GFAP):c.406C>T (p.Arg136Trp)
NM_002055.5(GFAP):c.575C>T (p.Ser192Leu)
NM_002055.5(GFAP):c.599T>C (p.Leu200Ser)
NM_002055.5(GFAP):c.643C>G (p.Leu215Val)
NM_002055.5(GFAP):c.737C>T (p.Ala246Val)	rs374224631

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