List of variants in gene combination LMNA, LOC129931597 reported as uncertain significance for hereditary skeletal muscle disorder

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.74G>T (p.Arg25Leu)	rs61578124	0.00002
NM_170707.4(LMNA):c.23G>A (p.Arg8His)	rs1329278578	0.00001
NM_170707.4(LMNA):c.65C>T (p.Ser22Leu)	rs1016767319	0.00001
NM_170707.4(LMNA):c.71C>T (p.Thr24Ile)	rs1195524446	0.00001
NM_170707.4(LMNA):c.104T>A (p.Leu35Gln)
NM_170707.4(LMNA):c.41C>T (p.Ala14Val)
NM_170707.4(LMNA):c.47C>A (p.Ala16Asp)	rs770799870
NM_170707.4(LMNA):c.64T>C (p.Ser22Pro)
NM_170707.4(LMNA):c.89A>C (p.Gln30Pro)
NM_170707.4(LMNA):c.91del (p.Glu31fs)

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