Variants in gene MAGEL2 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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: 5

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HGVS	dbSNP	gnomAD frequency
NM_019066.5(MAGEL2):c.1021C>T (p.Gln341Ter)	rs2140717169
NM_019066.5(MAGEL2):c.1621C>T (p.Gln541Ter)	rs1555374290
NM_019066.5(MAGEL2):c.1808C>G (p.Ser603Ter)	rs1595332731
NM_019066.5(MAGEL2):c.1912C>T (p.Gln638Ter)	rs797044883
NM_019066.5(MAGEL2):c.2057G>A (p.Trp686Ter)	rs768844200

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