List of variants in gene combination GFAP, LOC130060994 reported as not provided by Epithelial Biology; Institute of Medical Biology, Singapore

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_002055.5(GFAP):c.1070T>C (p.Leu357Pro)	rs267607515
NM_002055.5(GFAP):c.1075C>G (p.Leu359Val)	rs60825166
NM_002055.5(GFAP):c.1076T>C (p.Leu359Pro)	rs267607511
NM_002055.5(GFAP):c.1079A>T (p.Asp360Val)	rs62636501
NM_002055.5(GFAP):c.1086G>C (p.Glu362Asp)	rs121909718
NM_002055.5(GFAP):c.1090G>C (p.Ala364Pro)	rs58645997
NM_002055.5(GFAP):c.1091C>T (p.Ala364Val)	rs267607503
NM_002055.5(GFAP):c.1096T>C (p.Tyr366His)	rs58008462
NM_002055.5(GFAP):c.1097A>G (p.Tyr366Cys)	rs267607502
NM_002055.5(GFAP):c.1111G>C (p.Glu371Gln)	rs267607526
NM_002055.5(GFAP):c.1112A>G (p.Glu371Gly)	rs57815192
NM_002055.5(GFAP):c.1112A>T (p.Glu371Val)	rs57815192
NM_002055.5(GFAP):c.1117G>A (p.Glu373Lys)	rs58075601
NM_002055.5(GFAP):c.1117G>C (p.Glu373Gln)	rs58075601
NM_002055.5(GFAP):c.1121A>G (p.Glu374Gly)	rs59628143
NM_002055.5(GFAP):c.1126C>G (p.Arg376Gly)	rs267607512
NM_002055.5(GFAP):c.1126C>T (p.Arg376Trp)	rs267607512

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