ClinVar Miner

List of variants in gene CHRNA2 reported as benign by Invitae

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_000742.4(CHRNA2):c.373A>G (p.Thr125Ala) rs891398 0.58886
NM_000742.4(CHRNA2):c.351C>T (p.Asp117=) rs2565061 0.17492
NM_000742.4(CHRNA2):c.65C>T (p.Thr22Ile) rs2472553 0.16614
NM_000742.4(CHRNA2):c.1324C>T (p.Leu442=) rs56298562 0.01760
NM_000742.4(CHRNA2):c.913C>T (p.Leu305=) rs114294066 0.01308
NM_000742.4(CHRNA2):c.771C>T (p.Tyr257=) rs56229264 0.01257
NM_000742.4(CHRNA2):c.1434C>A (p.Asp478Glu) rs56344740 0.00307
NM_000742.4(CHRNA2):c.449+12T>C rs202012980 0.00236
NM_000742.4(CHRNA2):c.1500C>T (p.Ile500=) rs143223159 0.00150
NM_000742.4(CHRNA2):c.1100G>A (p.Arg367Gln) rs149464248 0.00091
NM_000742.4(CHRNA2):c.684C>T (p.Ser228=) rs143536618 0.00073
NM_000742.4(CHRNA2):c.987C>T (p.Gly329=) rs147530139 0.00055
NM_000742.4(CHRNA2):c.1437C>T (p.His479=) rs374849310 0.00025
NM_000742.4(CHRNA2):c.401G>A (p.Arg134Lys) rs150112824 0.00013
NM_000742.4(CHRNA2):c.1432G>A (p.Asp478Asn) rs141072985 0.00006
NM_000742.4(CHRNA2):c.930C>T (p.Phe310=) rs554976506 0.00002
NM_000742.4(CHRNA2):c.489C>T (p.Ala163=) rs535699325 0.00001
NM_000742.4(CHRNA2):c.295-16_295-7dup rs776047724
NM_000742.4(CHRNA2):c.339+12_339+13del rs139680977
NM_000742.4(CHRNA2):c.339+13dup rs139680977
NM_000742.4(CHRNA2):c.340-16C>A

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