List of variants reported as likely benign for progeria

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Total variants: 40

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HGVS	dbSNP	gnomAD frequency
NM_001143985.1(BANF1):c.-254G>T	rs78790365	0.02064
NM_007055.4(POLR3A):c.1724A>T (p.Lys575Met)	rs56214655	0.01630
NM_170707.4(LMNA):c.51C>T (p.Ser17=)	rs11549668	0.00797
NM_170707.4(LMNA):c.612G>A (p.Leu204=)	rs12117552	0.00637
NM_007055.4(POLR3A):c.2938A>G (p.Ile980Val)	rs146253630	0.00599
NM_003860.4(BANF1):c.*100C>T	rs145574018	0.00424
NM_170707.4(LMNA):c.811-13T>A	rs80356809	0.00309
NM_001143985.1(BANF1):c.-297G>A	rs141605220	0.00271
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.-128T>C	rs80356803	0.00051
NM_001143985.1(BANF1):c.-408C>T	rs117774800	0.00044
NM_003860.4(BANF1):c.*273C>G	rs142270527	0.00037
NM_170707.4(LMNA):c.1584G>A (p.Thr528=)	rs80356812	0.00029
NM_170707.4(LMNA):c.811-12C>T	rs372962650	0.00012
NM_170707.4(LMNA):c.1488+7G>A	rs374209100	0.00007
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.1299C>T (p.His433=)	rs61217436	0.00004
NM_170707.4(LMNA):c.1380+18G>A	rs777846700	0.00003
NM_170707.4(LMNA):c.1381-13A>G	rs750192865	0.00003
NM_170707.4(LMNA):c.1698+57G>A	rs557334569	0.00002
NM_170707.4(LMNA):c.1857T>C (p.Ser619=)	rs368581237	0.00002
NM_170707.4(LMNA):c.1155G>A (p.Glu385=)	rs878855232	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.153G>T (p.Ser51=)	rs751886390	0.00001
NM_170707.4(LMNA):c.1662G>A (p.Glu554=)	rs201936898	0.00001
NM_170707.4(LMNA):c.1699-9C>T	rs776616872	0.00001
NM_170707.4(LMNA):c.1731T>C (p.Ala577=)	rs776066211	0.00001
NM_170707.4(LMNA):c.369G>A (p.Lys123=)	rs367938270	0.00001
NM_170707.4(LMNA):c.96G>A (p.Lys32=)	rs775429079	0.00001
NM_007055.4(POLR3A):c.1745G>T (p.Arg582Leu)	rs34588967
NM_170707.4(LMNA):c.-88G>T	rs115800510
NM_170707.4(LMNA):c.1381-6C>G	rs371635492
NM_170707.4(LMNA):c.1485G>A (p.Val495=)	rs1651703234
NM_170707.4(LMNA):c.1551G>A (p.Gln517=)	rs41314035
NM_170707.4(LMNA):c.1659C>T (p.Asp553=)	rs748768783
NM_170707.4(LMNA):c.1968+18dup	rs554157057
NM_170707.4(LMNA):c.927C>A (p.Leu309=)	rs752558753

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