List of variants in gene combination LMNA, LOC126805877 reported by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.438C>T (p.Ala146=)	rs80356805	0.00782
NM_170707.4(LMNA):c.357C>T (p.Arg119=)	rs41313880	0.00321
NM_170707.4(LMNA):c.370G>A (p.Glu124Lys)	rs2102865393
NM_170707.4(LMNA):c.449C>T (p.Thr150Ile)	rs869069617
NM_170707.4(LMNA):c.470C>A (p.Thr157Lys)
NM_170707.4(LMNA):c.481G>A (p.Glu161Lys)	rs28933093

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