Variants in gene ATL1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (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_015915.5(ATL1):c.351G>A (p.Glu117=)	rs1060197	0.79691
NM_015915.5(ATL1):c.84A>G (p.Pro28=)	rs35014209	0.18809
NM_015915.5(ATL1):c.669C>T (p.Tyr223=)	rs146975855	0.00059
NM_015915.5(ATL1):c.991-6T>G	rs192428744	0.00016
NM_015915.5(ATL1):c.1173C>T (p.His391=)	rs149340140	0.00013
NM_015915.5(ATL1):c.306C>A (p.Asp102Glu)	rs145204580	0.00010
NM_015915.5(ATL1):c.921C>T (p.Pro307=)	rs535790981	0.00001

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