ClinVar Miner

List of variants in gene LMNB2 reported as benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (69):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_032737.4(LMNB2):c.1416T>C (p.Gly472=) rs11084940 0.59479
NM_032737.4(LMNB2):c.1590+14C>T rs115439379 0.01154
NM_032737.4(LMNB2):c.704G>A (p.Arg235Gln) rs121912497 0.01005
NM_032737.4(LMNB2):c.1822-17T>C rs201909206 0.00184
NM_032737.4(LMNB2):c.804C>T (p.Asp268=) rs150969746 0.00159
NM_032737.4(LMNB2):c.1482+15C>T rs199890540 0.00120
NM_032737.4(LMNB2):c.1483-11G>A rs191041189 0.00086
NM_032737.4(LMNB2):c.265-19C>T rs199577453 0.00046
NM_032737.4(LMNB2):c.1751G>A (p.Arg584His) rs377036714 0.00034
NM_032737.4(LMNB2):c.1247G>T (p.Arg416Leu) rs200293412 0.00025
NM_032737.4(LMNB2):c.700C>T (p.Arg234Trp) rs148936043 0.00025
NM_032737.4(LMNB2):c.1482+16G>A rs183380570 0.00021
NM_032737.4(LMNB2):c.685-5C>T rs369839679 0.00019
NM_032737.4(LMNB2):c.1681C>T (p.Arg561Cys) rs751633226 0.00018
NM_032737.4(LMNB2):c.1482+11A>T rs202063885 0.00015
NM_032737.4(LMNB2):c.1483-20G>A rs371984370 0.00014
NM_032737.4(LMNB2):c.1063G>A (p.Ala355Thr) rs143717863 0.00011
NM_032737.4(LMNB2):c.1378G>A (p.Gly460Ser) rs566078588 0.00010
NM_032737.4(LMNB2):c.514G>A (p.Gly172Ser) rs145110937 0.00009
NM_032737.4(LMNB2):c.1711-7C>T rs200122476 0.00008
NM_032737.4(LMNB2):c.403G>A (p.Ala135Thr) rs372474156 0.00008
NM_032737.4(LMNB2):c.1279G>A (p.Ala427Thr) rs57521499 0.00007
NM_032737.4(LMNB2):c.1407G>A (p.Ser469=) rs200879771 0.00007
NM_032737.4(LMNB2):c.1483-12C>T rs761892602 0.00006
NM_032737.4(LMNB2):c.1821+4G>A rs779811801 0.00004
NM_032737.4(LMNB2):c.750G>C (p.Gln250His) rs758373595 0.00004
NM_032737.4(LMNB2):c.395A>G (p.Asn132Ser) rs780297843 0.00003
NM_032737.4(LMNB2):c.1711-3C>T rs777181580 0.00002
NM_032737.4(LMNB2):c.1482+20C>T rs763504322 0.00001
NM_032737.4(LMNB2):c.624G>A (p.Leu208=) rs1305321896 0.00001
NM_032737.4(LMNB2):c.1232G>A (p.Arg411His) rs138467082
NM_032737.4(LMNB2):c.1554G>C (p.Thr518=) rs11882908
NM_032737.4(LMNB2):c.1612G>C (p.Val538Leu) rs2145444752
NM_032737.4(LMNB2):c.1629C>G (p.Pro543=) rs149126950
NM_032737.4(LMNB2):c.1677C>G (p.Ser559Arg)
NM_032737.4(LMNB2):c.1682G>A (p.Arg561His) rs145444042
NM_032737.4(LMNB2):c.1682G>T (p.Arg561Leu) rs145444042
NM_032737.4(LMNB2):c.1749G>A (p.Met583Ile) rs139812127
NM_032737.4(LMNB2):c.912C>A (p.Arg304=) rs202001996

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