List of variants in gene combination LMNA, LOC129931597 reported as likely benign for Charcot-Marie-Tooth disease type 2

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.74G>T (p.Arg25Leu)	rs61578124	0.00003
NM_170707.4(LMNA):c.78C>T (p.Ile26=)	rs373721390	0.00003
NM_170707.4(LMNA):c.96G>A (p.Lys32=)	rs775429079	0.00002
NM_170707.4(LMNA):c.42G>A (p.Ala14=)	rs777460187	0.00001
NM_170707.4(LMNA):c.72C>T (p.Thr24=)	rs1572331957	0.00001
NM_170707.4(LMNA):c.93G>A (p.Glu31=)	rs878855235	0.00001
NM_170707.4(LMNA):c.102C>T (p.Asp34=)	rs2527830824
NM_170707.4(LMNA):c.103C>T (p.Leu35=)	rs56694480
NM_170707.4(LMNA):c.21G>A (p.Arg7=)	rs2102816901
NM_170707.4(LMNA):c.21G>C (p.Arg7=)	rs2102816901
NM_170707.4(LMNA):c.24C>A (p.Arg8=)	rs1337375663
NM_170707.4(LMNA):c.36C>T (p.Ser12=)
NM_170707.4(LMNA):c.39G>A (p.Gly13=)	rs747663457
NM_170707.4(LMNA):c.66G>A (p.Ser22=)	rs886043729
NM_170707.4(LMNA):c.75C>T (p.Arg25=)	rs80356804
NM_170707.4(LMNA):c.87G>T (p.Leu29=)	rs2527830495
NM_170707.4(LMNA):c.90G>A (p.Gln30=)	rs1325971304

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