"PreventionGenetics, part of Exact Sciences"[submitter] AND "KCNB2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3052365	NM_004770.3(KCNB2):c.81T>C (p.Ile27=)	KCNB2	Single nucleotide variant (synonymous variant)	KCNB2-related disorder	GLikely benign
Select item 770572	NM_004770.3(KCNB2):c.156G>T (p.Thr52=)	KCNB2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1282555	NM_004770.3(KCNB2):c.171C>G (p.Pro57=)	KCNB2	Single nucleotide variant (synonymous variant)	KCNB2-related disorder +1 more	GBenign
Select item 3057267	NM_004770.3(KCNB2):c.1944C>G (p.Gly648=)	KCNB2	Single nucleotide variant (synonymous variant)	KCNB2-related disorder	GLikely benign
Select item 3037129	NM_004770.3(KCNB2):c.2178A>C (p.Ala726=)	KCNB2	Single nucleotide variant (synonymous variant)	KCNB2-related disorder	GBenign
Select item 3050997	NM_004770.3(KCNB2):c.2567C>T (p.Pro856Leu)	KCNB2 (P856L)	Single nucleotide variant (missense variant)	KCNB2-related disorder	GLikely benign
Select item 1226816	NM_004770.3(KCNB2):c.2613G>A (p.Val871=)	KCNB2	Single nucleotide variant (synonymous variant)	KCNB2-related disorder +1 more	GBenign

ClinVar