List of variants in gene LMNA, LOC129931597 studied for Cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.51C>T (p.Ser17=)	rs11549668	0.00797
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.20G>A (p.Arg7Gln)	rs751916168	0.00001
NM_170707.4(LMNA):c.23G>A (p.Arg8His)	rs1329278578	0.00001
NM_170707.4(LMNA):c.42G>A (p.Ala14=)	rs777460187	0.00001
NM_170707.4(LMNA):c.65C>T (p.Ser22Leu)	rs1016767319	0.00001
NM_170707.4(LMNA):c.93G>A (p.Glu31=)	rs878855235	0.00001
NM_170707.4(LMNA):c.105G>C (p.Leu35=)
NM_170707.4(LMNA):c.24C>A (p.Arg8=)	rs1337375663
NM_170707.4(LMNA):c.25G>A (p.Ala9Thr)	rs2527829229
NM_170707.4(LMNA):c.37G>A (p.Gly13Arg)	rs1649700208
NM_170707.4(LMNA):c.39G>A (p.Gly13=)	rs747663457
NM_170707.4(LMNA):c.71C>G (p.Thr24Ser)	rs1195524446
NM_170707.4(LMNA):c.72C>G (p.Thr24=)	rs1572331957
NM_170707.4(LMNA):c.76A>C (p.Ile26Leu)	rs1302425397

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