ClinVar Miner

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

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_032737.4(LMNB2):c.1029C>T (p.Ala343=) rs749052582
NM_032737.4(LMNB2):c.1332C>T (p.Pro444=) rs998616364
NM_032737.4(LMNB2):c.1344C>T (p.Gly448=) rs144665669
NM_032737.4(LMNB2):c.1363G>C (p.Gly455Arg) rs772769360
NM_032737.4(LMNB2):c.1575C>T (p.Ala525=) rs140216957
NM_032737.4(LMNB2):c.1698C>T (p.Asn566=) rs147619532
NM_032737.4(LMNB2):c.1707C>T (p.Gly569=) rs372581793
NM_032737.4(LMNB2):c.1776G>A (p.Glu592=) rs1555682686
NM_032737.4(LMNB2):c.264+7G>T rs748398790
NM_032737.4(LMNB2):c.815G>A (p.Arg272Gln) rs142557433
NM_032737.4(LMNB2):c.906G>A (p.Ala302=) rs144417417
NM_032737.4(LMNB2):c.982-4G>A rs370025312

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