List of variants in gene CHRNA4 reported as uncertain significance 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: 24

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HGVS	dbSNP	gnomAD frequency
NM_000744.7(CHRNA4):c.77-4G>A	rs201123897	0.00141
NM_000744.7(CHRNA4):c.1108C>T (p.Arg370Trp)	rs76378652	0.00080
NM_000744.7(CHRNA4):c.1441G>A (p.Gly481Ser)	rs111969225	0.00070
NM_000744.7(CHRNA4):c.1203G>C (p.Leu401=)	rs56142348	0.00066
NM_000744.7(CHRNA4):c.1006C>T (p.Arg336Cys)	rs56175056	0.00045
NM_000744.7(CHRNA4):c.1560C>T (p.Leu520=)	rs142646795	0.00027
NM_000744.7(CHRNA4):c.1635G>A (p.Thr545=)	rs121912283	0.00021
NM_000744.7(CHRNA4):c.1715A>G (p.Gln572Arg)	rs113794453	0.00011
NM_000744.7(CHRNA4):c.729G>A (p.Pro243=)	rs121912253	0.00009
NM_000744.7(CHRNA4):c.1494C>T (p.Ala498=)	rs137860047	0.00007
NM_000744.7(CHRNA4):c.1454G>A (p.Arg485Gln)	rs755416498	0.00006
NM_000744.7(CHRNA4):c.1327C>G (p.His443Asp)	rs796052319	0.00003
NM_000744.7(CHRNA4):c.1685C>T (p.Pro562Leu)	rs200750362	0.00002
NM_000744.7(CHRNA4):c.1495G>A (p.Ala499Thr)	rs150336658	0.00001
NM_000744.7(CHRNA4):c.1634C>T (p.Thr545Met)	rs121912282	0.00001
NM_000744.7(CHRNA4):c.1842G>A (p.Thr614=)	rs727503871	0.00001
NM_000744.7(CHRNA4):c.412C>T (p.Leu138=)	rs372063405	0.00001
NM_000744.7(CHRNA4):c.758C>T (p.Pro253Leu)	rs747083728	0.00001
NM_000744.7(CHRNA4):c.868C>T (p.Leu290=)	rs762952445	0.00001
NM_000744.7(CHRNA4):c.1517C>A (p.Ala506Asp)	rs1317311176
NM_000744.7(CHRNA4):c.1653C>A (p.Thr551=)	rs886043995
NM_000744.7(CHRNA4):c.466A>G (p.Ile156Val)	rs754895704
NM_000744.7(CHRNA4):c.681C>A (p.Ala227=)	rs45588436
NM_000744.7(CHRNA4):c.904dup (p.Val302fs)	rs1568809897

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