List of variants in gene LMNA reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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.811-13T>A	rs80356809	0.00309
NM_170707.4(LMNA):c.1761G>A (p.Leu587=)	rs80356813	0.00210
NM_170707.4(LMNA):c.1566C>T (p.Cys522=)	rs149339264	0.00123
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.192C>T (p.Thr64=)	rs137969290	0.00028
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.1770C>T (p.Thr590=)	rs397517896	0.00006
NM_170707.4(LMNA):c.1803C>T (p.Ser601=)	rs267607604	0.00005
NM_170707.4(LMNA):c.726G>A (p.Ala242=)	rs763625309	0.00004
NM_170707.4(LMNA):c.1227A>G (p.Thr409=)	rs762130433	0.00003
NM_170707.4(LMNA):c.1699-7T>C	rs771074100	0.00003
NM_170707.4(LMNA):c.1098G>A (p.Lys366=)	rs57901307	0.00002
NM_170707.4(LMNA):c.1719G>A (p.Ser573=)	rs759853354	0.00002
NM_170707.4(LMNA):c.1755C>T (p.Thr585=)	rs545752475	0.00002
NM_170707.4(LMNA):c.153G>T (p.Ser51=)	rs751886390	0.00001
NM_170707.4(LMNA):c.1785C>T (p.Ala595=)	rs748139390	0.00001
NM_170707.4(LMNA):c.*694A>G
NM_170707.4(LMNA):c.1179T>C (p.Pro393=)	rs1651603737
NM_170707.4(LMNA):c.138C>T (p.Ile46=)	rs1553261914
NM_170707.4(LMNA):c.1551G>A (p.Gln517=)	rs41314035
NM_170707.4(LMNA):c.1770C>G (p.Thr590=)	rs397517896
NM_170707.4(LMNA):c.1968+62G>T
NM_170707.4(LMNA):c.1968+80G>T
NM_170707.4(LMNA):c.528A>G (p.Leu176=)

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