Variants in gene ALDH7A1 with conflicting interpretations "likely pathogenic" and "uncertain significance"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_001182.5(ALDH7A1):c.34del (p.Ala12fs)	rs750693623	0.00057
NM_001182.5(ALDH7A1):c.529G>C (p.Ala177Pro)	rs140102105	0.00006
NM_001182.5(ALDH7A1):c.1556G>A (p.Arg519Lys)	rs561343926	0.00004
NM_001182.5(ALDH7A1):c.664A>G (p.Thr222Ala)	rs777829351	0.00003
NM_001182.5(ALDH7A1):c.575C>T (p.Thr192Met)	rs376917645	0.00001
NM_001182.5(ALDH7A1):c.607T>G (p.Trp203Gly)	rs555896752	0.00001
NM_001182.5(ALDH7A1):c.1301A>G (p.Tyr434Cys)	rs747597620
NM_001182.5(ALDH7A1):c.1439T>C (p.Ile480Thr)	rs886059849
NM_001182.5(ALDH7A1):c.494G>T (p.Gly165Val)	rs375491094
NM_001182.5(ALDH7A1):c.826A>C (p.Thr276Pro)	rs796052260

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