List of variants in gene CREBBP reported as likely pathogenic by Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004380.3(CREBBP):c.1094A>C (p.His365Pro)
NM_004380.3(CREBBP):c.1930G>C (p.Ala644Pro)	rs2141237064
NM_004380.3(CREBBP):c.2031del (p.Ile678fs)	rs1555483716
NM_004380.3(CREBBP):c.5186G>C (p.Cys1729Ser)	rs2051863859

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