List of variants in gene CWC27 reported as likely pathogenic by Fulgent Genetics, Fulgent Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_005869.4(CWC27):c.938+2T>C	rs767210188	0.00001
NM_005869.4(CWC27):c.139+2T>C
NM_005869.4(CWC27):c.397-1G>A	rs2112169750
NM_005869.4(CWC27):c.756del (p.Gly253fs)	rs2112207891
NM_005869.4(CWC27):c.829del (p.Glu277fs)
NM_005869.4(CWC27):c.872del (p.Lys291fs)

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