List of variants in gene ALDH7A1 reported as benign by Illumina Laboratory Services, Illumina

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001182.5(ALDH7A1):c.*807C>G	rs1807	0.60056
NM_001182.5(ALDH7A1):c.*2499G>A	rs7715516	0.52610
NM_001182.5(ALDH7A1):c.*1749G>T	rs744722	0.43746
NM_001182.5(ALDH7A1):c.*1748T>A	rs744721	0.43127
NM_001182.5(ALDH7A1):c.*68A>G	rs2775	0.42285
NM_001182.5(ALDH7A1):c.*726C>T	rs1060857	0.37480
NM_001182.4(ALDH7A1):c.-132A>C	rs900641	0.24797
NM_001182.4(ALDH7A1):c.-151C>T	rs900640	0.11028
NM_001182.5(ALDH7A1):c.1315A>C (p.Lys439Gln)	rs12514417	0.08598
NM_001182.5(ALDH7A1):c.273T>C (p.Thr91=)	rs60720055	0.06152
NM_001182.4(ALDH7A1):c.-60G>A	rs144272515	0.03685
NM_001182.5(ALDH7A1):c.518-12T>G	rs79544459	0.03492
NM_001182.5(ALDH7A1):c.*2254T>A	rs76249070	0.02408
NM_001182.5(ALDH7A1):c.675C>T (p.Leu225=)	rs57902950	0.01833
NM_001182.5(ALDH7A1):c.*1804C>T	rs744723	0.01339
NM_001182.5(ALDH7A1):c.*1672A>G	rs78029541	0.01247
NM_001182.5(ALDH7A1):c.*1741T>A	rs744720	0.01233
NM_001182.5(ALDH7A1):c.*1368A>T	rs115645125	0.01210
NM_001182.5(ALDH7A1):c.*2512G>A	rs76363408	0.00874
NM_001182.5(ALDH7A1):c.*1446G>A	rs114580465	0.00797
NM_001182.5(ALDH7A1):c.*2575T>C	rs114287342	0.00792
NM_001182.5(ALDH7A1):c.*2423C>T	rs114575585	0.00777
NM_001182.4(ALDH7A1):c.-117G>T	rs146562077	0.00663
NM_001182.5(ALDH7A1):c.1234A>G (p.Thr412Ala)	rs2306618	0.00250
NM_001182.5(ALDH7A1):c.373A>G (p.Ile125Val)	rs117295656	0.00144
NM_001182.5(ALDH7A1):c.*1702del	rs5871218
NM_001182.5(ALDH7A1):c.*2997dup	rs5871217
NM_001182.5(ALDH7A1):c.*3022T>C	rs2035471
NM_001182.5(ALDH7A1):c.*818G>A	rs1138005

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