ClinVar Miner

List of variants in gene LMNA reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 120
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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.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.1930C>T (p.Arg644Cys) rs142000963 0.00117
NM_170707.4(LMNA):c.1804G>A (p.Gly602Ser) rs60662302 0.00078
NM_170707.4(LMNA):c.1911C>T (p.Phe637=) rs117939448 0.00048
NM_170707.4(LMNA):c.789G>A (p.Leu263=) rs148557956 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.1656C>T (p.Asp552=) rs370219874 0.00016
NM_170707.4(LMNA):c.895A>G (p.Ile299Val) rs150924946 0.00016
NM_170707.4(LMNA):c.1051A>C (p.Arg351=) rs771623461 0.00013
NM_170707.4(LMNA):c.1488+14C>T rs377700689 0.00013
NM_170707.4(LMNA):c.811-12C>T rs372962650 0.00012
NM_170707.4(LMNA):c.990G>A (p.Glu330=) rs140800215 0.00012
NM_170707.4(LMNA):c.1314G>A (p.Gly438=) rs774817302 0.00011
NM_170707.4(LMNA):c.150C>T (p.Arg50=) rs397517894 0.00009
NM_170707.4(LMNA):c.1243G>A (p.Val415Ile) rs267607606 0.00007
NM_170707.4(LMNA):c.1488+7G>A rs374209100 0.00007
NM_170707.4(LMNA):c.1530C>T (p.Thr510=) rs138098342 0.00007
NM_170707.4(LMNA):c.1149G>A (p.Glu383=) rs267607603 0.00006
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.1311C>T (p.Ser437=) rs763224059 0.00004
NM_170707.4(LMNA):c.726G>A (p.Ala242=) rs763625309 0.00004
NM_170707.4(LMNA):c.936+12C>T rs199881992 0.00004
NM_170707.4(LMNA):c.1227A>G (p.Thr409=) rs762130433 0.00003
NM_170707.4(LMNA):c.1317C>A (p.Arg439=) rs374804871 0.00003
NM_170707.4(LMNA):c.1362G>A (p.Leu454=) rs151160622 0.00003
NM_170707.4(LMNA):c.1381-13A>G rs750192865 0.00003
NM_170707.4(LMNA):c.1908C>T (p.Ser636=) rs80356814 0.00003
NM_170707.4(LMNA):c.885G>A (p.Ser295=) rs776999079 0.00003
NM_170707.4(LMNA):c.1038C>T (p.Ala346=) rs1019030652 0.00002
NM_170707.4(LMNA):c.1047G>A (p.Arg349=) rs147015659 0.00002
NM_170707.4(LMNA):c.1071C>T (p.Asp357=) rs376875762 0.00002
NM_170707.4(LMNA):c.1098G>A (p.Lys366=) rs57901307 0.00002
NM_170707.4(LMNA):c.1158-12C>G rs372934817 0.00002
NM_170707.4(LMNA):c.1236G>C (p.Gly412=) rs763537103 0.00002
NM_170707.4(LMNA):c.1755C>T (p.Thr585=) rs545752475 0.00002
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.867C>T (p.His289=) rs780415585 0.00002
NM_170707.4(LMNA):c.937-9C>T rs1332011298 0.00002
NM_170707.4(LMNA):c.111G>A (p.Glu37=) rs886038906 0.00001
NM_170707.4(LMNA):c.1138T>C (p.Leu380=) rs1215331296 0.00001
NM_170707.4(LMNA):c.1182C>T (p.Thr394=) rs1409406468 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.153G>T (p.Ser51=) rs751886390 0.00001
NM_170707.4(LMNA):c.1605G>A (p.Gly535=) rs769398087 0.00001
NM_170707.4(LMNA):c.1662G>A (p.Glu554=) rs201936898 0.00001
NM_170707.4(LMNA):c.1680C>T (p.Asp560=) rs17847249 0.00001
NM_170707.4(LMNA):c.1699-9C>T rs776616872 0.00001
NM_170707.4(LMNA):c.1728C>T (p.Pro576=) rs767783294 0.00001
NM_170707.4(LMNA):c.1731T>C (p.Ala577=) rs776066211 0.00001
NM_170707.4(LMNA):c.1764C>T (p.Cys588=) rs759016336 0.00001
NM_170707.4(LMNA):c.1773C>T (p.Cys591=) rs397517897 0.00001
NM_170707.4(LMNA):c.1785C>T (p.Ala595=) rs748139390 0.00001
NM_170707.4(LMNA):c.1890G>A (p.Gly630=) rs770389147 0.00001
NM_170707.4(LMNA):c.540G>A (p.Lys180=) rs1437725392 0.00001
NM_170707.4(LMNA):c.573G>A (p.Val191=) rs754525930 0.00001
NM_170707.4(LMNA):c.606G>A (p.Glu202=) rs963378138 0.00001
NM_170707.4(LMNA):c.643C>T (p.Leu215=) rs397517905 0.00001
NM_170707.4(LMNA):c.678G>A (p.Leu226=) rs964377328 0.00001
NM_170707.4(LMNA):c.771G>A (p.Glu257=) rs1471649557 0.00001
NM_170707.4(LMNA):c.870G>A (p.Glu290=) rs747275587 0.00001
NM_170707.4(LMNA):c.948G>A (p.Lys316=) rs778421025 0.00001
NM_170707.4(LMNA):c.1005G>C (p.Arg335=)
NM_170707.4(LMNA):c.1029G>C (p.Arg343=) rs1553265680
NM_170707.4(LMNA):c.1045C>A (p.Arg349=)
NM_170707.4(LMNA):c.1062G>A (p.Gln354=)
NM_170707.4(LMNA):c.1083G>A (p.Glu361=) rs1651569117
NM_170707.4(LMNA):c.1104C>T (p.Ala368=)
NM_170707.4(LMNA):c.1122C>T (p.His374=) rs143715750
NM_170707.4(LMNA):c.1173C>T (p.Pro391=) rs1553265807
NM_170707.4(LMNA):c.1185G>T (p.Ser395=) rs397517890
NM_170707.4(LMNA):c.1209C>T (p.Ser403=) rs776975256
NM_170707.4(LMNA):c.1218A>G (p.Ser406=) rs1651612863
NM_170707.4(LMNA):c.1302A>G (p.Ala434=)
NM_170707.4(LMNA):c.1305C>T (p.Arg435=)
NM_170707.4(LMNA):c.1317C>T (p.Arg439=) rs374804871
NM_170707.4(LMNA):c.1323C>T (p.Ala441=) rs140194535
NM_170707.4(LMNA):c.138C>T (p.Ile46=) rs1553261914
NM_170707.4(LMNA):c.1536G>A (p.Leu512=) rs1208359364
NM_170707.4(LMNA):c.1551G>A (p.Gln517=) rs41314035
NM_170707.4(LMNA):c.1578G>T (p.Leu526=) rs1205674172
NM_170707.4(LMNA):c.1599C>T (p.Ser533=) rs886043346
NM_170707.4(LMNA):c.1677T>C (p.Asp559=)
NM_170707.4(LMNA):c.1725C>T (p.Asp575=)
NM_170707.4(LMNA):c.1749G>A (p.Ser583=) rs970494454
NM_170707.4(LMNA):c.1749G>C (p.Ser583=)
NM_170707.4(LMNA):c.1794A>G (p.Ala598=)
NM_170707.4(LMNA):c.1800C>T (p.Ala600=)
NM_170707.4(LMNA):c.1806C>T (p.Gly602=)
NM_170707.4(LMNA):c.1818G>A (p.Gln606=) rs1060504514
NM_170707.4(LMNA):c.1827A>T (p.Gly609=) rs1558135172
NM_170707.4(LMNA):c.1860C>T (p.Val620=)
NM_170707.4(LMNA):c.1887G>C (p.Val629=)
NM_170707.4(LMNA):c.1890G>C (p.Gly630=) rs770389147
NM_170707.4(LMNA):c.1914G>A (p.Gly638=)
NM_170707.4(LMNA):c.1941C>T (p.Leu647=) rs984562109
NM_170707.4(LMNA):c.1971C>T (p.Ser657=) rs1023544978
NM_170707.4(LMNA):c.207G>C (p.Val69=) rs886038801
NM_170707.4(LMNA):c.657G>A (p.Lys219=) rs1553265267
NM_170707.4(LMNA):c.711T>C (p.Phe237=) rs768081358
NM_170707.4(LMNA):c.729T>C (p.Asp243=) rs753243743
NM_170707.4(LMNA):c.750C>T (p.Ala250=) rs2102881551
NM_170707.4(LMNA):c.774G>A (p.Gln258=) rs2102881783
NM_170707.4(LMNA):c.807C>T (p.Ala269=)
NM_170707.4(LMNA):c.873G>A (p.Glu291=)
NM_170707.4(LMNA):c.888C>T (p.Arg296=)
NM_170707.4(LMNA):c.897C>T (p.Ile299=) rs762718963
NM_170707.4(LMNA):c.927C>A (p.Leu309=) rs752558753
NM_170707.4(LMNA):c.930G>A (p.Gln310=)
NM_170707.4(LMNA):c.937-15C>T
NM_170707.4(LMNA):c.945C>G (p.Ala315=)
NM_170707.4(LMNA):c.945C>T (p.Ala315=)

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