List of variants in gene CHRNA4 reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000744.7(CHRNA4):c.1448G>A (p.Arg483Gln)	rs55855125	0.00016
NM_000744.7(CHRNA4):c.1583C>T (p.Pro528Leu)	rs201739273	0.00006
NM_000744.7(CHRNA4):c.442C>T (p.Arg148Trp)	rs121912243	0.00003
NM_000744.7(CHRNA4):c.1158_1160delinsGGG (p.Glu387Gly)	rs796052320
NM_000744.7(CHRNA4):c.1209_1210delinsTT (p.Pro404Ser)	rs1064795858
NM_000744.7(CHRNA4):c.1220C>T (p.Ser407Phe)	rs761335733
NM_000744.7(CHRNA4):c.1369G>A (p.Ala457Thr)	rs753598324
NM_000744.7(CHRNA4):c.1726G>C (p.Asp576His)	rs537904499
NM_000744.7(CHRNA4):c.1759-17G>C

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