List of variants in gene ALDH4A1 reported as likely 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_003748.4(ALDH4A1):c.*35C>T	rs2230710	0.02193
NM_003748.4(ALDH4A1):c.744C>T (p.Ile248=)	rs60427141	0.01815
NM_003748.4(ALDH4A1):c.1631C>T (p.Pro544Leu)	rs72953172	0.01344
NM_003748.4(ALDH4A1):c.1162T>C (p.Phe388Leu)	rs41273175	0.01334
NM_003748.4(ALDH4A1):c.*903C>T	rs148846466	0.01203
NM_003748.4(ALDH4A1):c.584C>T (p.Thr195Met)	rs72936434	0.00992
NM_003748.4(ALDH4A1):c.433G>A (p.Ala145Thr)	rs113846237	0.00952
NM_003748.4(ALDH4A1):c.*657del	rs11311839
NM_003748.4(ALDH4A1):c.1086G>A (p.Pro362=)	rs41310410

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