Variants in gene KCNA5 with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002234.4(KCNA5):c.913G>A (p.Ala305Thr)	rs199794307	0.00007
NM_002234.4(KCNA5):c.1580C>T (p.Thr527Met)	rs121908591	0.00005
NM_002234.4(KCNA5):c.1727C>T (p.Ala576Val)	rs121908592	0.00001

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