List of variants in gene FIG4 reported as likely benign by GeneDx

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: 51

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HGVS	dbSNP	gnomAD frequency
NC_000006.12:g.109825565A>G	rs76385456	0.02142
NM_014845.6(FIG4):c.2097-217C>T	rs78154984	0.01518
NM_014845.6(FIG4):c.2546+158C>T	rs7745191	0.01508
NM_014845.6(FIG4):c.1949-148A>G	rs115395338	0.01355
NM_014845.5(FIG4):c.-182G>A	rs55873083	0.01220
NM_014845.6(FIG4):c.776-270C>T	rs112727135	0.01149
NM_014845.6(FIG4):c.1434+54G>A	rs57159750	0.01033
NM_014845.6(FIG4):c.497+61G>A	rs115467680	0.00992
NM_014845.6(FIG4):c.1138-284A>G	rs111341099	0.00891
NM_014845.6(FIG4):c.497+175A>T	rs111759494	0.00875
NM_014845.6(FIG4):c.1584-30A>C	rs116602685	0.00742
NM_014845.6(FIG4):c.498-87T>C	rs112790444	0.00683
NM_014845.6(FIG4):c.1138-291G>A	rs113252524	0.00678
NM_014845.6(FIG4):c.1751-294A>G	rs59852203	0.00670
NM_014845.6(FIG4):c.2377-71T>G	rs186543204	0.00563
NM_014845.6(FIG4):c.498-145A>G	rs192762300	0.00456
NM_014845.6(FIG4):c.*14C>T	rs114136062	0.00408
NM_014845.6(FIG4):c.1389-209T>G	rs148001811	0.00366
NM_014845.6(FIG4):c.647-48C>T	rs114219763	0.00352
NM_014845.6(FIG4):c.1889+309T>C	rs182955642	0.00305
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.834A>T (p.Lys278Asn)	rs138048706	0.00029
NM_014845.6(FIG4):c.1305G>C (p.Val435=)	rs145227623	0.00011
NM_014845.6(FIG4):c.1863C>A (p.Thr621=)	rs201744761	0.00011
NM_014845.6(FIG4):c.1138-45A>T	rs201459736	0.00009
NM_014845.6(FIG4):c.2459+7T>G	rs575271308	0.00009
NM_014845.6(FIG4):c.66+13dup	rs755637236	0.00007
NM_014845.6(FIG4):c.1040-4T>C	rs374343214	0.00004
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.1620C>T (p.Thr540=)	rs746367416	0.00002
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.1812A>G (p.Lys604=)	rs1399930708	0.00001
NM_014845.6(FIG4):c.2460-17T>C	rs201533992	0.00001
NM_014845.6(FIG4):c.1435-117TTTTTG[7]	rs71018366
NM_014845.6(FIG4):c.1583+3A>G	rs866431185
NM_014845.6(FIG4):c.165+228C>T	rs73535344
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.2459+59C>T	rs77634668
NM_014845.6(FIG4):c.2546+17A>C	rs1050332219
NM_014845.6(FIG4):c.2547-5T>G	rs200267243
NM_014845.6(FIG4):c.289+280A>G	rs73535347
NM_014845.6(FIG4):c.447-17dup	rs764540259
NM_014845.6(FIG4):c.447-4_447-3dup	rs11377100

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