Variants in gene combination GATAD1, PEX1 with conflicting interpretations reported as "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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000466.3(PEX1):c.2966T>C (p.Ile989Thr)	rs61750427	0.00003
NM_000466.3(PEX1):c.2845C>T (p.Arg949Trp)	rs866184460	0.00001
NM_000466.3(PEX1):c.2926+2T>C	rs267608180	0.00001
NM_000466.3(PEX1):c.3208-1G>A	rs1057517518	0.00001
NM_000466.3(PEX1):c.2798dup (p.Pro934fs)	rs1057517484
NM_000466.3(PEX1):c.2852dup (p.His951fs)	rs767877383
NM_000466.3(PEX1):c.2859dup (p.Thr954fs)	rs1057517472
NM_000466.3(PEX1):c.2875C>T (p.Arg959Ter)	rs1057517481
NM_000466.3(PEX1):c.2916del (p.Gly973fs)	rs61750426
NM_000466.3(PEX1):c.2922del (p.Leu974fs)	rs762324548
NM_000466.3(PEX1):c.2992C>T (p.Arg998Ter)	rs61750428
NM_000466.3(PEX1):c.3115del (p.Thr1039fs)	rs1562846257
NM_000466.3(PEX1):c.3303_3304dup (p.Cys1102fs)	rs886043558
NM_000466.3(PEX1):c.3329_3332del (p.Val1109_Ser1110insTer)	rs1585214453
NM_000466.3(PEX1):c.3455_3456del (p.Ser1152fs)	rs759183382
NM_000466.3(PEX1):c.3574C>T (p.Gln1192Ter)	rs1057517467
NM_000466.3(PEX1):c.3693_3696del (p.Gln1231fs)	rs769836601

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