List of variants in gene combination CYP1B1, LOC128772254 reported as likely pathogenic for not provided

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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_000104.4(CYP1B1):c.1310C>T (p.Pro437Leu)	rs56175199	0.00005
NM_000104.4(CYP1B1):c.1390dup (p.Ser464fs)	rs777515179
NM_000104.4(CYP1B1):c.1403_1429dup (p.Arg468_Ser476dup)	rs72549373
NM_000104.4(CYP1B1):c.1426T>C (p.Ser476Pro)	rs1682416281

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