Variants in gene KCNB1 with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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_004975.4(KCNB1):c.1142G>A (p.Gly381Glu)	rs1569017114
NM_004975.4(KCNB1):c.1237G>A (p.Val413Ile)	rs1984243311
NM_004975.4(KCNB1):c.877C>T (p.Arg293Cys)	rs1984264748
NM_004975.4(KCNB1):c.898C>T (p.Arg300Cys)	rs202170806
NM_004975.4(KCNB1):c.986A>G (p.Asn329Ser)	rs1984257387

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