List of variants in gene FUS reported as likely benign by Illumina Laboratory Services, Illumina

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_004960.4(FUS):c.*41G>A	rs80301724	0.00551
NM_004960.3(FUS):c.*1992A>C	rs146490489	0.00325
NM_004960.3(FUS):c.*1998T>C	rs182437252	0.00272
NM_004960.3(FUS):c.*2005G>T	rs140979886	0.00123
NM_004960.3(FUS):c.*335G>T	rs192206514	0.00076
NM_004960.3(FUS):c.*561C>T	rs192705444	0.00058
NM_004960.4(FUS):c.404G>A (p.Ser135Asn)	rs61732970	0.00056
NM_004960.3(FUS):c.*1089G>A	rs184277413	0.00025
NM_004960.4(FUS):c.1080C>T (p.Ser360=)	rs190724342	0.00022
NM_004960.3(FUS):c.*1286C>G	rs547623704	0.00016
NM_004960.4(FUS):c.687T>C (p.Gly229=)	rs781445592	0.00014
NM_004960.4(FUS):c.1169-11A>G	rs181859716	0.00010
NM_004960.3(FUS):c.*1375C>T	rs542241137	0.00007
NM_004960.4(FUS):c.1348C>T (p.Pro450Ser)	rs201533156	0.00003
NM_004960.3(FUS):c.*2348G>A	rs775218493	0.00001
NM_004960.3(FUS):c.1145_1146delCA	rs1211904015
NM_004960.3(FUS):c.*2955A>G	rs149361851
NM_004960.3(FUS):c.*814T>C	rs772679520
NM_004960.4(FUS):c.*132C>A	rs565540429
NM_004960.4(FUS):c.1292+22dup	rs572228309
NM_004960.4(FUS):c.669CGG[7] (p.Gly231dup)	rs72550890

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