List of variants in gene combination CDH23, LOC111982869 reported as likely pathogenic for endocrine gland neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.7903G>T (p.Val2635Phe)	rs763721044	0.00002
NM_022124.6(CDH23):c.7899C>G (p.Tyr2633Ter)	rs1375264465	0.00001
NM_022124.6(CDH23):c.7987TTC[1] (p.Phe2664del)	rs774559018
NM_022124.6(CDH23):c.8064+1G>T	rs1474524543

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