Variants in gene GDAP1 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_018972.4(GDAP1):c.487C>T (p.Gln163Ter)	rs104894077	0.00015
NM_018972.4(GDAP1):c.692C>T (p.Pro231Leu)	rs121908114	0.00015
NM_018972.4(GDAP1):c.458C>T (p.Pro153Leu)	rs538412810	0.00001
NM_018972.4(GDAP1):c.193G>A (p.Glu65Lys)	rs1808862287
NM_018972.4(GDAP1):c.194A>G (p.Glu65Gly)	rs2131496131
NM_018972.4(GDAP1):c.482G>A (p.Arg161His)	rs104894076
NM_018972.4(GDAP1):c.571C>T (p.Arg191Ter)	rs1554547986
NM_018972.4(GDAP1):c.817C>G (p.Arg273Gly)	rs150989205
NM_018972.4(GDAP1):c.818G>A (p.Arg273Gln)	rs879254192

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