Variants in gene KCNB1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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_004975.4(KCNB1):c.1182G>A (p.Gly394=)	rs77238446	0.00481
NM_004975.4(KCNB1):c.1389T>A (p.Ile463=)	rs115929614	0.00239
NM_004975.4(KCNB1):c.1296G>A (p.Arg432=)	rs142605642	0.00097
NM_004975.4(KCNB1):c.1734G>C (p.Gly578=)	rs145456546	0.00081
NM_004975.4(KCNB1):c.2136G>A (p.Thr712=)	rs139458439	0.00057
NM_004975.4(KCNB1):c.1576G>A (p.Val526Ile)	rs140932636	0.00034
NM_004975.4(KCNB1):c.375C>T (p.Asp125=)	rs201414449	0.00004
NM_004975.4(KCNB1):c.1880G>A (p.Arg627Gln)	rs754927664

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