List of variants in gene LMNA reported as likely benign by Molecular Genetics Laboratory, London Health Sciences Centre

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.1761G>A (p.Leu587=)	rs80356813	0.00210
NM_170707.4(LMNA):c.1851C>T (p.Ala617=)	rs143189394	0.00158
NM_170707.4(LMNA):c.1566C>T (p.Cys522=)	rs149339264	0.00123
NM_170707.4(LMNA):c.1489-16C>G	rs201379016	0.00076
NM_170707.4(LMNA):c.1911C>T (p.Phe637=)	rs117939448	0.00048
NM_170707.4(LMNA):c.1584G>A (p.Thr528=)	rs80356812	0.00029
NM_170707.4(LMNA):c.1017G>A (p.Ala339=)	rs17847242	0.00021
NM_170707.4(LMNA):c.1488+14C>T	rs377700689	0.00013
NM_170707.4(LMNA):c.1314G>A (p.Gly438=)	rs774817302	0.00011
NM_170707.4(LMNA):c.1770C>T (p.Thr590=)	rs397517896	0.00006
NM_170707.4(LMNA):c.937-7C>G	rs267607681	0.00006
NM_170707.4(LMNA):c.936+12C>T	rs199881992	0.00004
NM_170707.4(LMNA):c.1857T>C (p.Ser619=)	rs368581237	0.00002
NM_170707.4(LMNA):c.579T>C (p.Ala193=)	rs749728556	0.00002
NM_170707.4(LMNA):c.810+12C>T	rs746914371	0.00002
NM_170707.4(LMNA):c.1092C>T (p.Asp364=)	rs776589077	0.00001
NM_170707.4(LMNA):c.1157+15C>T	rs761166147	0.00001
NM_170707.4(LMNA):c.1157+19G>A	rs757715731	0.00001
NM_170707.4(LMNA):c.12G>A (p.Pro4=)	rs369823958	0.00001
NM_170707.4(LMNA):c.1488+8G>A	rs762836610	0.00001
NM_170707.4(LMNA):c.1699-8C>G	rs727503137	0.00001
NM_170707.4(LMNA):c.1969-4T>C	rs751715969	0.00001
NM_170707.4(LMNA):c.1261C>T (p.Leu421=)	rs1194745110
NM_170707.4(LMNA):c.1551G>A (p.Gln517=)	rs41314035
NM_170707.4(LMNA):c.1968+18dup	rs554157057
NM_170707.4(LMNA):c.572T>G (p.Val191Gly)	rs752087253

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