List of variants in gene FUS reported as benign by Athena Diagnostics Inc

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_004960.4(FUS):c.291C>T (p.Tyr97=)	rs1052352	0.45484
NM_004960.4(FUS):c.147C>A (p.Gly49=)	rs741810	0.24179
NM_004960.4(FUS):c.1156C>A (p.Arg386=)	rs61733965	0.01496
NM_004960.4(FUS):c.524-5C>T	rs73530287	0.01495
NM_004960.4(FUS):c.1566G>A (p.Arg522=)	rs138901914	0.00095
NM_004960.4(FUS):c.404G>A (p.Ser135Asn)	rs61732970	0.00056
NM_004960.4(FUS):c.1248C>T (p.Gly416=)	rs368780804	0.00005
NM_004960.4(FUS):c.1541+9_1541+10del	rs761850706
NM_004960.4(FUS):c.669CGG[7] (p.Gly231dup)	rs72550890

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