List of variants in gene CYP7B1 reported as benign 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_004820.5(CYP7B1):c.1234-208C>T	rs7822429	0.95183
NM_004820.5(CYP7B1):c.259+281A>T	rs13251633	0.68123
NM_004820.5(CYP7B1):c.123-72A>G	rs73237769	0.08641
NM_004820.5(CYP7B1):c.850+159T>A	rs73689557	0.06676
NM_004820.5(CYP7B1):c.1233+70C>T	rs6991989	0.04415
NM_004820.5(CYP7B1):c.56T>C (p.Leu19Pro)	rs72554624	0.04177
NM_004820.5(CYP7B1):c.1058-140C>T	rs79377721	0.02495
NM_004820.5(CYP7B1):c.1058-142C>T	rs79219323	0.02494
NM_004820.5(CYP7B1):c.123-9del	rs8192895
NM_004820.5(CYP7B1):c.1234-99_1234-88del	rs112410433
NM_004820.5(CYP7B1):c.260-15dup	rs8192896
NM_004820.5(CYP7B1):c.260-5del	rs8192896
NM_004820.5(CYP7B1):c.850+157A>T	rs4543580
NM_004820.5(CYP7B1):c.850+158dup	rs8192897
NM_004820.5(CYP7B1):c.851-204C>T	rs73237765

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