List of variants in gene CHRNA1 reported as likely benign for not provided

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: 36

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HGVS	dbSNP	gnomAD frequency
NC_000002.12:g.174764492G>A	rs35274388	0.02247
NM_000079.4(CHRNA1):c.344+74G>A	rs35759748	0.01175
NM_000079.4(CHRNA1):c.778+316C>G	rs112943369	0.01174
NM_000079.4(CHRNA1):c.345-130C>T	rs142609209	0.00884
NM_000079.4(CHRNA1):c.*426C>A	rs115375214	0.00774
NM_000079.4(CHRNA1):c.345-98C>T	rs113375495	0.00757
NM_000079.4(CHRNA1):c.779-124C>T	rs76427148	0.00712
NM_000079.4(CHRNA1):c.1002+120C>T	rs10208554	0.00698
NM_000079.4(CHRNA1):c.235-518C>G	rs13391443	0.00696
NM_000079.4(CHRNA1):c.778+145C>T	rs753193	0.00676
NM_000079.4(CHRNA1):c.778+201G>A	rs77490322	0.00601
NM_000079.4(CHRNA1):c.*218C>T	rs79539026	0.00579
NM_000079.4(CHRNA1):c.1233G>T (p.Glu411Asp)	rs61737716	0.00561
NM_000079.4(CHRNA1):c.*499A>T	rs574135903	0.00488
NM_000079.4(CHRNA1):c.234+33T>C	rs78091507	0.00470
NM_000079.4(CHRNA1):c.643G>A (p.Asp215Asn)	rs148304857	0.00413
NM_000079.4(CHRNA1):c.-8G>A	rs138563328	0.00270
NM_000079.4(CHRNA1):c.655C>T (p.Leu219=)	rs150638770	0.00220
NM_000079.4(CHRNA1):c.621C>T (p.Ser207=)	rs74533173	0.00185
NM_000079.4(CHRNA1):c.224G>A (p.Arg75His)	rs147488907	0.00069
NM_000079.4(CHRNA1):c.1064A>G (p.Glu355Gly)	rs144533405	0.00065
NM_000079.4(CHRNA1):c.1293C>T (p.Leu431=)	rs146899588	0.00054
NM_000079.4(CHRNA1):c.546C>T (p.Ser182=)	rs749002411	0.00016
NM_000079.4(CHRNA1):c.372G>A (p.Lys124=)	rs143047599	0.00009
NM_000079.4(CHRNA1):c.723C>T (p.Pro241=)	rs189442556	0.00008
NM_000079.4(CHRNA1):c.813G>A (p.Leu271=)	rs374093236	0.00007
NM_000079.4(CHRNA1):c.735C>T (p.Phe245=)	rs773397465	0.00001
NM_000079.4(CHRNA1):c.204G>A (p.Gln68=)	rs886043372
NM_000079.4(CHRNA1):c.235-358T>C	rs867184330
NM_000079.4(CHRNA1):c.411G>A (p.Thr137=)
NM_000079.4(CHRNA1):c.44-118G>A	rs76603995
NM_000079.4(CHRNA1):c.516C>T (p.Asp172=)
NM_000079.4(CHRNA1):c.618C>T (p.His206=)	rs757820359
NM_000079.4(CHRNA1):c.705C>T (p.Ile235=)
NM_000079.4(CHRNA1):c.779-15_779-12del	rs67309103
NM_000079.4(CHRNA1):c.779-28dup	rs67309103

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