List of variants in gene CYP26B1 reported as uncertain significance for bone development disease

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_019885.4(CYP26B1):c.1179G>T (p.Met393Ile)	rs1341772264	0.00001
NM_019885.4(CYP26B1):c.344C>T (p.Thr115Ile)	rs1281765906	0.00001
NM_019885.4(CYP26B1):c.74_77dup (p.Val28fs)	rs771651519	0.00001
NM_019885.4(CYP26B1):c.1333C>T (p.His445Tyr)	rs1676614895
NM_019885.4(CYP26B1):c.584G>A (p.Arg195Gln)

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