List of variants in gene combination CHRNA4, LOC100130587 reported 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
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000744.7(CHRNA4):c.51G>A (p.Leu17=)	rs79739740	0.05992
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.44T>C (p.Leu15Pro)	rs886044055

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