List of variants in gene FHL1 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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001159699.2(FHL1):c.204+5C>T	rs182106777	0.00542
NM_001159699.2(FHL1):c.489C>T (p.Asp163=)	rs149670651	0.00162
NM_001159699.2(FHL1):c.786C>T (p.His262=)	rs141231353	0.00074
NM_001159699.2(FHL1):c.114G>A (p.Lys38=)	rs140149764	0.00067
NM_001159699.2(FHL1):c.225C>A (p.Arg75=)	rs143791173	0.00037
NM_001159702.3(FHL1):c.-101+10C>G	rs1013945435	0.00034
NM_001159699.2(FHL1):c.331C>T (p.Arg111Trp)	rs150911744	0.00030
NM_001159699.2(FHL1):c.736+8A>G	rs376754350	0.00007
NM_001159699.2(FHL1):c.550-15C>A	rs764137409	0.00005
NM_001159702.3(FHL1):c.-109C>A	rs1556630646	0.00005
NM_001159702.3(FHL1):c.-27+17G>T	rs367650287	0.00005
NM_001159699.2(FHL1):c.380-16T>C	rs772665517	0.00004
NM_001159699.2(FHL1):c.651C>T (p.Thr217=)	rs370597064	0.00004
NM_001159699.2(FHL1):c.737-5C>A	rs771803774	0.00004
NM_001159699.2(FHL1):c.549+7T>G	rs771700018	0.00003
NM_001159699.2(FHL1):c.179G>A (p.Arg60His)	rs11557264	0.00002
NM_001159699.2(FHL1):c.205-9G>C	rs1178092343	0.00002
NM_001159699.2(FHL1):c.519G>A (p.Lys173=)	rs750331409	0.00001
NM_001159699.2(FHL1):c.537G>C (p.Val179=)	rs753535765	0.00001
NM_001159699.2(FHL1):c.549+5G>A	rs747714932	0.00001
NM_001159699.2(FHL1):c.736+18T>C	rs774416768	0.00001
NM_001159699.2(FHL1):c.737-14T>C	rs769912263	0.00001
NM_001159699.2(FHL1):c.789C>T (p.Asp263=)	rs1057523997	0.00001
NM_001159699.2(FHL1):c.618C>G (p.Thr206=)	rs1556639368
NM_001159699.2(FHL1):c.736+14T>C	rs1556639409
NM_001159699.2(FHL1):c.737-3del	rs368428875
NM_001159699.2(FHL1):c.737-9del	rs374867802
NM_001159699.2(FHL1):c.855G>A (p.Glu285=)	rs1556639756
NM_001159702.3(FHL1):c.-108C>T	rs1158663274

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