List of variants in gene CYP26B1 reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_019885.4(CYP26B1):c.572G>A (p.Arg191His)	rs76025186	0.00293
NM_019885.4(CYP26B1):c.454G>A (p.Glu152Lys)	rs143622603	0.00091
NM_019885.4(CYP26B1):c.1040C>T (p.Thr347Met)	rs200556766	0.00009
NM_019885.4(CYP26B1):c.1505C>T (p.Pro502Leu)	rs375261360	0.00006
NM_019885.4(CYP26B1):c.1443C>A (p.His481Gln)	rs781553628	0.00004
NM_019885.4(CYP26B1):c.344C>T (p.Thr115Ile)	rs1281765906	0.00001
NM_019885.4(CYP26B1):c.1085T>C (p.Met362Thr)
NM_019885.4(CYP26B1):c.1208C>T (p.Ala403Val)	rs1309087026
NM_019885.4(CYP26B1):c.1417C>A (p.Arg473Ser)	rs61751056
NM_019885.4(CYP26B1):c.628C>G (p.Leu210Val)	rs1441876570

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