List of variants in gene BAP1 reported as likely pathogenic by Color Diagnostics, LLC DBA Color Health

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004656.4(BAP1):c.1891-1G>A	rs1705011794
NM_004656.4(BAP1):c.2056+1G>C	rs1578218644
NM_004656.4(BAP1):c.255+1G>A	rs1060503750
NM_004656.4(BAP1):c.256-2A>C	rs2153228161
NM_004656.4(BAP1):c.376-1G>A	rs2153227978
NM_004656.4(BAP1):c.437+1G>T	rs1553645838
NM_004656.4(BAP1):c.438-1G>A	rs2153227879
NM_004656.4(BAP1):c.784-2A>T	rs1559589344

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