List of variants in gene CWC27 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_005869.4(CWC27):c.1152+2T>A	rs747658761	0.00006
NM_005869.4(CWC27):c.938+2T>C	rs767210188	0.00001
NC_000005.9:g.(?_64077833)_(64174102_?)del
NC_000005.9:g.(?_64267510)_(64273085_?)dup
NM_005869.4(CWC27):c.1153-1G>C
NM_005869.4(CWC27):c.252+1G>A
NM_005869.4(CWC27):c.600-9_606del
NM_005869.4(CWC27):c.749+1G>T

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