Variants in gene PDHA1 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000284.4(PDHA1):c.1100A>C (p.His367Pro)	rs1131691584
NM_000284.4(PDHA1):c.1142_1145dup (p.Trp383fs)	rs606231189
NM_000284.4(PDHA1):c.214C>T (p.Arg72Cys)	rs863224148
NM_000284.4(PDHA1):c.379C>T (p.Arg127Trp)	rs199959402
NM_000284.4(PDHA1):c.491A>G (p.Asn164Ser)	rs1555933963
NM_000284.4(PDHA1):c.615C>G (p.Phe205Leu)	rs137853254
NM_000284.4(PDHA1):c.692C>G (p.Thr231Arg)	rs1272572107
NM_000284.4(PDHA1):c.936_939del (p.Ser312fs)	rs863224153

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