ClinVar Miner

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

Included ClinVar conditions (88):
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Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NM_000742.4(CHRNA2):c.*1003G>A rs74974243
NM_000742.4(CHRNA2):c.*1006G>A rs145560154
NM_000742.4(CHRNA2):c.*108C>T rs147882344
NM_000742.4(CHRNA2):c.*1117G>A
NM_000742.4(CHRNA2):c.*1159T>C rs1560344
NM_000742.4(CHRNA2):c.*1384C>T rs2280376
NM_000742.4(CHRNA2):c.*1392A>G rs564765220
NM_000742.4(CHRNA2):c.*1403C>G rs376282591
NM_000742.4(CHRNA2):c.*1446A>G rs28697263
NM_000742.4(CHRNA2):c.*1480C>T rs113471592
NM_000742.4(CHRNA2):c.*1667G>A
NM_000742.4(CHRNA2):c.*1701C>A rs1057137
NM_000742.4(CHRNA2):c.*1809T>C rs2280375
NM_000742.4(CHRNA2):c.*1849A>G rs531828656
NM_000742.4(CHRNA2):c.*285G>C rs111565880
NM_000742.4(CHRNA2):c.*29G>A rs186509115
NM_000742.4(CHRNA2):c.*384G>A rs76428534
NM_000742.4(CHRNA2):c.*511G>C rs2292977
NM_000742.4(CHRNA2):c.*602T>C rs2292976
NM_000742.4(CHRNA2):c.*623G>A rs79796894
NM_000742.4(CHRNA2):c.*721G>T rs2292975
NM_000742.4(CHRNA2):c.*755G>A rs2292974
NM_000742.4(CHRNA2):c.*771C>T rs572058986
NM_000742.4(CHRNA2):c.*936C>T rs112587531
NM_000742.4(CHRNA2):c.-379T>C rs75861520
NM_000742.4(CHRNA2):c.-422G>A rs80025940
NM_000742.4(CHRNA2):c.-424C>T rs55726427
NM_000742.4(CHRNA2):c.-447T>A rs75312501
NM_000742.4(CHRNA2):c.-448G>A rs78426134
NM_000742.4(CHRNA2):c.-45C>A rs12114756
NM_000742.4(CHRNA2):c.-561A>T rs111661898
NM_000742.4(CHRNA2):c.-563T>A rs2565060
NM_000742.4(CHRNA2):c.1099C>T (p.Arg367Trp) rs751699392
NM_000742.4(CHRNA2):c.1234G>A (p.Glu412Lys) rs141721605
NM_000742.4(CHRNA2):c.1324C>T (p.Leu442=) rs56298562
NM_000742.4(CHRNA2):c.140C>T (p.Thr47Met) rs74772771
NM_000742.4(CHRNA2):c.1434C>A (p.Asp478Glu) rs56344740
NM_000742.4(CHRNA2):c.1437C>T (p.His479=) rs374849310
NM_000742.4(CHRNA2):c.1500C>T (p.Ile500=) rs143223159
NM_000742.4(CHRNA2):c.1530C>T (p.Ile510=) rs149142237
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.202C>T (p.Arg68Trp) rs376970816
NM_000742.4(CHRNA2):c.295-16_295-7dup rs776047724
NM_000742.4(CHRNA2):c.340-15C>A rs373046238
NM_000742.4(CHRNA2):c.351C>T (p.Asp117=) rs2565061
NM_000742.4(CHRNA2):c.373A>G (p.Thr125Ala) rs891398
NM_000742.4(CHRNA2):c.449+12T>C rs202012980
NM_000742.4(CHRNA2):c.45C>T (p.Ser15=) rs149934219
NM_000742.4(CHRNA2):c.489C>T (p.Ala163=) rs535699325
NM_000742.4(CHRNA2):c.65C>T (p.Thr22Ile) rs2472553
NM_000742.4(CHRNA2):c.684C>T (p.Ser228=) rs143536618
NM_000742.4(CHRNA2):c.745G>A (p.Ala249Thr) rs77710085
NM_000742.4(CHRNA2):c.771C>T (p.Tyr257=) rs56229264
NM_000742.4(CHRNA2):c.913C>T (p.Leu305=) rs114294066
NM_000742.4(CHRNA2):c.930C>T (p.Phe310=) rs554976506

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