List of variants in gene LMNA reported as likely benign for Hutchinson-Gilford syndrome

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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.612G>A (p.Leu204=)	rs12117552	0.00637
NM_170707.4(LMNA):c.811-13T>A	rs80356809	0.00309
NM_170707.4(LMNA):c.1566C>T (p.Cys522=)	rs149339264	0.00123
NM_170707.4(LMNA):c.-128T>C	rs80356803	0.00051
NM_170707.4(LMNA):c.1584G>A (p.Thr528=)	rs80356812	0.00029
NM_170707.4(LMNA):c.1149G>A (p.Glu383=)	rs267607603	0.00006
NM_170707.4(LMNA):c.1488G>A (p.Thr496=)	rs375516745	0.00005
NM_170707.4(LMNA):c.1698+57G>A	rs557334569	0.00002
NM_170707.4(LMNA):c.-88G>T	rs115800510
NM_170707.4(LMNA):c.1551G>A (p.Gln517=)	rs41314035

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