List of variants in gene GFAP reported as benign for not specified

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_002055.5(GFAP):c.1171+471C>T	rs78994946	0.02110
NM_002055.5(GFAP):c.469G>A (p.Asp157Asn)	rs59291670	0.01088
NM_002055.5(GFAP):c.96T>C (p.Gly32=)	rs60045579	0.00844
NM_002055.5(GFAP):c.738G>A (p.Ala246=)	rs147404772	0.00624
NM_002055.5(GFAP):c.140C>T (p.Pro47Leu)	rs57474185	0.00543
NM_002055.5(GFAP):c.720G>T (p.Thr240=)	rs2229012	0.00494
NM_002055.5(GFAP):c.313C>T (p.Arg105Trp)	rs139838162	0.00244
NM_002055.5(GFAP):c.1171+459_1171+460inv
NM_002055.5(GFAP):c.462-8dup	rs572562362

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