List of variants in gene combination ALDH4A1, LOC129929550 reported as uncertain significance for hyperprolinemia type 2

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_003748.4(ALDH4A1):c.16C>T (p.Pro6Ser)	rs1212781668	0.00001
NM_003748.4(ALDH4A1):c.12_17del (p.4PA[1])	rs768891033
NM_003748.4(ALDH4A1):c.1A>G (p.Met1Val)
NM_003748.4(ALDH4A1):c.43C>G (p.Arg15Gly)	rs2100625391
NM_003748.4(ALDH4A1):c.43C>T (p.Arg15Cys)
NM_003748.4(ALDH4A1):c.59C>A (p.Ala20Asp)	rs1935834310

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