ClinVar Miner

List of variants in gene CHRNA2 reported as likely benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (88):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_000742.4(CHRNA2):c.1123C>G (p.Pro375Ala) rs746613509
NM_000742.4(CHRNA2):c.1176C>T (p.Pro392=) rs764346961
NM_000742.4(CHRNA2):c.1234G>A (p.Glu412Lys) rs141721605
NM_000742.4(CHRNA2):c.1248G>C (p.Val416=) rs370878600
NM_000742.4(CHRNA2):c.1317C>T (p.His439=) rs775578495
NM_000742.4(CHRNA2):c.1335G>C (p.Gly445=) rs544902151
NM_000742.4(CHRNA2):c.140C>T (p.Thr47Met) rs74772771
NM_000742.4(CHRNA2):c.1410G>A (p.Leu470=) rs1586388697
NM_000742.4(CHRNA2):c.1464+7_1464+8del rs763426344
NM_000742.4(CHRNA2):c.150G>T (p.Pro50=) rs758848783
NM_000742.4(CHRNA2):c.1530C>T (p.Ile510=) rs149142237
NM_000742.4(CHRNA2):c.1551C>T (p.Ile517=) rs777412930
NM_000742.4(CHRNA2):c.166A>T (p.Thr56Ser) rs144185168
NM_000742.4(CHRNA2):c.173C>T (p.Thr58Ile) rs151268950
NM_000742.4(CHRNA2):c.210C>T (p.Tyr70=) rs144316375
NM_000742.4(CHRNA2):c.222G>A (p.Ala74=) rs369806823
NM_000742.4(CHRNA2):c.225C>T (p.Arg75=) rs371737919
NM_000742.4(CHRNA2):c.246C>T (p.Asp82=) rs201244136
NM_000742.4(CHRNA2):c.276C>T (p.Ile92=) rs201944711
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.609C>T (p.Ser203=) rs761237311
NM_000742.4(CHRNA2):c.699C>T (p.Ile233=) rs1321895505
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.759C>T (p.Pro253=) rs144913811
NM_000742.4(CHRNA2):c.772G>A (p.Ala258Thr) rs200372256
NM_000742.4(CHRNA2):c.790C>T (p.Leu264=) rs746292157
NM_000742.4(CHRNA2):c.795G>A (p.Pro265=) rs756903177
NM_000742.4(CHRNA2):c.852G>A (p.Val284=) rs1357751027
NM_000742.4(CHRNA2):c.873C>T (p.Ser291=) rs76140563
NM_000742.4(CHRNA2):c.966G>A (p.Ser322=) rs140118184
NM_000742.4(CHRNA2):c.984C>T (p.Ile328=) rs371858399

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