Related gene-specific medical variations for Gene (Select 10840) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109194	NM_012190.4(ALDH1L1):c.2585C>T (p.Thr862Met)	ALDH1L1, ALDH1L1-AS1 (T862M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109187	NM_012190.4(ALDH1L1):c.2449G>A (p.Asp817Asn)	ALDH1L1, ALDH1L1-AS1 (D716N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473739	NM_012190.4(ALDH1L1):c.2608G>A (p.Ala870Thr)	ALDH1L1, ALDH1L1-AS1 (A870T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397380	NM_012190.4(ALDH1L1):c.2467G>A (p.Val823Met)	ALDH1L1, ALDH1L1-AS1 (V722M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220787	NM_012190.4(ALDH1L1):c.2627A>G (p.Lys876Arg)	ALDH1L1, ALDH1L1-AS1 (K886R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 814479	GRCh37/hg19 3q21.3(chr3:125826729-126040939)x3	ALDH1L1	Copy number gain	not provided	GUncertain significance
Select item 784021	NM_012190.4(ALDH1L1):c.2503G>T (p.Ala835Ser)	ALDH1L1, ALDH1L1-AS1 (A845S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 713087	NM_012190.4(ALDH1L1):c.2453+6G>A	ALDH1L1, ALDH1L1-AS1	Single nucleotide variant (intron variant)	not provided	GBenign

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