List of variants in gene FIG4 reported as likely benign for not specified

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_014845.6(FIG4):c.447-16G>T	rs200890189	0.00618
NM_014845.6(FIG4):c.173A>G (p.Tyr58Cys)	rs145337669	0.00275
NM_014845.6(FIG4):c.446+9G>A	rs190287033	0.00128
NM_014845.6(FIG4):c.627A>G (p.Leu209=)	rs140111406	0.00119
NM_014845.6(FIG4):c.1584-8T>A	rs199522051	0.00086
NM_014845.6(FIG4):c.834A>T (p.Lys278Asn)	rs138048706	0.00029
NM_014845.6(FIG4):c.1863C>A (p.Thr621=)	rs201744761	0.00011
NM_014845.6(FIG4):c.2459+7T>G	rs575271308	0.00009
NM_014845.6(FIG4):c.1940A>G (p.Tyr647Cys)	rs150301327	0.00008
NM_014845.6(FIG4):c.66+13dup	rs755637236	0.00007
NM_014845.6(FIG4):c.1158T>C (p.His386=)	rs370557879	0.00004
NM_014845.6(FIG4):c.2199A>G (p.Glu733=)	rs537464083	0.00004
NM_014845.6(FIG4):c.33G>C (p.Ser11=)	rs527523781	0.00004
NM_014845.6(FIG4):c.1809G>A (p.Gly603=)	rs148280593	0.00002
NM_014845.6(FIG4):c.1949-15C>T	rs778444771	0.00002
NM_014845.6(FIG4):c.1272-16T>C	rs1554303954	0.00001
NM_014845.6(FIG4):c.1350C>G (p.Arg450=)	rs763035100	0.00001
NM_014845.6(FIG4):c.1812A>G (p.Lys604=)	rs1399930708	0.00001
NM_014845.6(FIG4):c.2238G>A (p.Pro746=)	rs753867543	0.00001
NM_014845.6(FIG4):c.2460-17T>C	rs201533992	0.00001
NM_014845.6(FIG4):c.497+14T>G	rs756070677	0.00001
NM_014845.6(FIG4):c.1751-3del	rs1064794667
NM_014845.6(FIG4):c.1770C>T (p.Ser590=)	rs1057524489
NM_014845.6(FIG4):c.1983G>A (p.Val661=)	rs1057524662
NM_014845.6(FIG4):c.2097-10C>G	rs142482745
NM_014845.6(FIG4):c.2377-11_2377-10del	rs200535694

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