Variants in gene ADSL with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000026.4(ADSL):c.358-4G>A	rs113199851	0.01950
NM_000026.4(ADSL):c.440A>T (p.Lys147Met)	rs11089991	0.01397
NM_000026.4(ADSL):c.124C>T (p.Leu42=)	rs2228415	0.00969
NM_000026.4(ADSL):c.1010+18A>G	rs201019280	0.00168
NM_000026.4(ADSL):c.403-4G>A	rs373652667	0.00064
NM_000026.4(ADSL):c.649C>G (p.His217Asp)	rs199761158	0.00024
NM_000026.4(ADSL):c.357+7G>A	rs199993991	0.00019

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