ClinVar Miner

List of variants in gene CHRNA2 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: 24
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HGVS dbSNP
NM_000742.4(CHRNA2):c.1158C>T (p.Pro386=) rs560790452
NM_000742.4(CHRNA2):c.1176C>T (p.Pro392=) rs764346961
NM_000742.4(CHRNA2):c.1248G>C (p.Val416=) rs370878600
NM_000742.4(CHRNA2):c.1378C>T (p.Leu460=) rs765948265
NM_000742.4(CHRNA2):c.140C>T (p.Thr47Met) rs74772771
NM_000742.4(CHRNA2):c.1464+7_1464+8del rs763426344
NM_000742.4(CHRNA2):c.1530C>T (p.Ile510=) rs149142237
NM_000742.4(CHRNA2):c.1569G>A (p.Pro523=) rs199993564
NM_000742.4(CHRNA2):c.210C>T (p.Tyr70=) rs144316375
NM_000742.4(CHRNA2):c.225C>A (p.Arg75=) rs371737919
NM_000742.4(CHRNA2):c.324C>T (p.Asn108=) rs544939077
NM_000742.4(CHRNA2):c.347G>T (p.Ser116Ile) rs541282922
NM_000742.4(CHRNA2):c.354C>T (p.Tyr118=) rs778279138
NM_000742.4(CHRNA2):c.383G>A (p.Gly128Asp) rs138682847
NM_000742.4(CHRNA2):c.45C>T (p.Ser15=) rs149934219
NM_000742.4(CHRNA2):c.710C>A (p.Thr237Lys) rs140350483
NM_000742.4(CHRNA2):c.723C>T (p.Asn241=) rs1060504822
NM_000742.4(CHRNA2):c.731A>G (p.Lys244Arg) rs146751925
NM_000742.4(CHRNA2):c.735C>T (p.Tyr245=) rs775595773
NM_000742.4(CHRNA2):c.745G>A (p.Ala249Thr) rs77710085
NM_000742.4(CHRNA2):c.790C>T (p.Leu264=) rs746292157
NM_000742.4(CHRNA2):c.852G>A (p.Val284=) rs1357751027
NM_000742.4(CHRNA2):c.966G>A (p.Ser322=) rs140118184
NM_000742.4(CHRNA2):c.984C>T (p.Ile328=) rs371858399

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