ClinVar Miner

List of variants in gene combination CHRNA4, LOC100130587 reported as benign by GeneDx

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Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_000744.7(CHRNA4):c.-182C>T rs191789990 0.62609
NM_000744.7(CHRNA4):c.76+157T>G rs11698563 0.47401
NM_000744.7(CHRNA4):c.-183C>T rs183345681 0.20643
NC_000020.11:g.63361542G>A rs12624510 0.07067
NC_000020.11:g.63361680C>T rs67568446 0.06524
NM_000744.7(CHRNA4):c.51G>A (p.Leu17=) rs79739740 0.05992
NM_000744.7(CHRNA4):c.76+95C>T rs62206940 0.03853
NM_000744.7(CHRNA4):c.24G>C (p.Ala8=) rs6089898 0.00898
NM_000744.7(CHRNA4):c.76+18G>T rs199908363 0.00504
NM_000744.7(CHRNA4):c.9A>G (p.Leu3=) rs80075498 0.00257
NM_000744.7(CHRNA4):c.42G>A (p.Pro14=) rs565990502 0.00048
NC_000020.11:g.63361453T>A rs58134915
NC_000020.11:g.63361486A>G rs13043186
NM_000744.7(CHRNA4):c.77-303G>C rs45568238

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