List of variants in gene CHRNA4 reported as benign by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_000744.7(CHRNA4):c.1227T>C (p.Cys409=)	rs2229960	0.86626
NM_000744.7(CHRNA4):c.678T>C (p.Cys226=)	rs1044394	0.80763
NM_000744.7(CHRNA4):c.639T>C (p.Asp213=)	rs1044393	0.78554
NM_000744.7(CHRNA4):c.1659G>A (p.Ala553=)	rs1044397	0.40553
NM_000744.7(CHRNA4):c.1629C>T (p.Ser543=)	rs1044396	0.40465
NM_000744.7(CHRNA4):c.1758+14A>G	rs3827020	0.19437
NM_000744.7(CHRNA4):c.1758+11C>T	rs45442394	0.04350
NM_000744.7(CHRNA4):c.1352C>T (p.Pro451Leu)	rs55915440	0.00262
NM_000744.7(CHRNA4):c.1401C>T (p.Ser467=)	rs45569837	0.00262
NM_000744.7(CHRNA4):c.1353G>A (p.Pro451=)	rs113168860	0.00222
NM_000744.7(CHRNA4):c.1143C>T (p.Ala381=)	rs75221202	0.00208
NM_000744.7(CHRNA4):c.1047G>A (p.Leu349=)	rs75593857	0.00200
NM_000744.7(CHRNA4):c.1758+16G>A	rs113109615	0.00153
NM_000744.7(CHRNA4):c.1460G>A (p.Arg487Gln)	rs121912280	0.00152
NM_000744.7(CHRNA4):c.978C>T (p.Phe326=)	rs76270730	0.00122
NM_000744.7(CHRNA4):c.402G>A (p.Ala134=)	rs201488442	0.00008
NM_000744.7(CHRNA4):c.1209G>T (p.Pro403=)	rs2229959

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