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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000026.4(ADSL):c.886C>T (p.Arg296Trp)	rs536254357	0.00004
NM_000026.4(ADSL):c.-21T>A	rs183190870	0.00002
NM_000026.4(ADSL):c.1027G>A (p.Glu343Lys)	rs774159147	0.00001
NM_000026.4(ADSL):c.1339T>C (p.Ser447Pro)	rs777821034	0.00001
NM_000026.4(ADSL):c.568C>G (p.Arg190Gly)	rs750614500
NM_000026.4(ADSL):c.859A>G (p.Ile287Val)	rs1209918065

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