"Clinical Genetics, Academic Medical Center"[submitter] AND "LOC126807 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 191559	NM_001148.6(ANK2):c.7007C>T (p.Ala2336Val)	ANK2, LOC126807137 (A2336V +4 more)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +4 more	GBenign
Select item 35690	NM_001148.6(ANK2):c.7106T>C (p.Val2369Ala)	ANK2, LOC126807137 (V2369A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified +5 more	GBenign/Likely benign
Select item 257582	NM_001148.6(ANK2):c.7110A>G (p.Gln2370=)	ANK2, LOC126807137	Single nucleotide variant (synonymous variant +1 more)	Cardiovascular phenotype +4 more	GBenign
Select item 703648	NM_001148.6(ANK2):c.7131C>T (p.Asp2377=)	ANK2, LOC126807137	Single nucleotide variant (synonymous variant +1 more)	Cardiovascular phenotype +1 more	GLikely benign
Select item 188143	NM_001148.6(ANK2):c.7132G>A (p.Glu2378Lys)	ANK2, LOC126807137 (E2378K +4 more)	Single nucleotide variant (intron variant +1 more)	Brugada syndrome +5 more	GConflicting classifications of pathogenicity
Select item 1089694	NM_001148.6(ANK2):c.7320C>T (p.Ser2440=)	ANK2, LOC126807137	Single nucleotide variant (synonymous variant +1 more)	Long QT syndrome +1 more	GLikely benign
Select item 238589	NM_001148.6(ANK2):c.7488A>G (p.Thr2496=)	ANK2, LOC126807137	Single nucleotide variant (synonymous variant +1 more)	ANK2-related disorder +5 more	GBenign/Likely benign

ClinVar