ClinVar Miner

List of variants in gene CHRNB2 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_000748.3(CHRNB2):c.1080C>A (p.Arg360=) rs1180459670
NM_000748.3(CHRNB2):c.1128C>T (p.Leu376=) rs113116986
NM_000748.3(CHRNB2):c.1233G>A (p.Ala411=) rs55857552
NM_000748.3(CHRNB2):c.1235G>A (p.Gly412Asp) rs112585933
NM_000748.3(CHRNB2):c.1236C>T (p.Gly412=) rs767533378
NM_000748.3(CHRNB2):c.1339-6A>T rs200177119
NM_000748.3(CHRNB2):c.1378C>G (p.Arg460Gly) rs202079239
NM_000748.3(CHRNB2):c.201C>T (p.Leu67=) rs773706734
NM_000748.3(CHRNB2):c.441G>A (p.Pro147=) rs780464481
NM_000748.3(CHRNB2):c.708C>T (p.Phe236=) rs71628622
NM_000748.3(CHRNB2):c.77C>T (p.Thr26Met) rs71651692
NM_000748.3(CHRNB2):c.780C>T (p.Ser260=) rs369234693

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