List of variants in gene FHL1 reported as benign for X-linked myopathy with postural muscle atrophy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001159699.2(FHL1):c.737-8C>T	rs2076705	0.53498
NM_001159699.2(FHL1):c.737-13T>C	rs11798700	0.01269
NM_001159699.2(FHL1):c.871G>A (p.Asp291Asn)	rs151315725	0.01175
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.498C>T (p.Cys166=)	rs145445372	0.00107
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.331C>T (p.Arg111Trp)	rs150911744	0.00030
NM_001159699.2(FHL1):c.737-9T>C	rs914754937	0.00022
NM_001159699.2(FHL1):c.380-16T>C	rs772665517	0.00004
NM_001159699.2(FHL1):c.737-5C>A	rs771803774	0.00004
NM_001159699.2(FHL1):c.737-3del	rs368428875
NM_001159699.2(FHL1):c.737-3dup
NM_001159699.2(FHL1):c.737-9del	rs374867802
NM_001159699.2(FHL1):c.737-9dup	rs374867802

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