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

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_015915.5(ATL1):c.1160T>C (p.Leu387Ser)	rs1595625010
NM_015915.5(ATL1):c.1217AGA[1] (p.Lys407del)	rs1595625099
NM_015915.5(ATL1):c.1220A>T (p.Lys407Met)	rs2039539459
NM_015915.5(ATL1):c.1243C>T (p.Arg415Trp)	rs119476050
NM_015915.5(ATL1):c.1306A>G (p.Asn436Asp)	rs2140239163
NM_015915.5(ATL1):c.466A>C (p.Thr156Pro)	rs2140205433
NM_015915.5(ATL1):c.715C>T (p.Arg239Cys)	rs119476046
NM_015915.5(ATL1):c.757G>A (p.Val253Ile)	rs864622520

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