List of variants in gene CRELD1 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001077415.3(CRELD1):c.959del (p.Gln320fs)	rs759473511	0.00035
NM_001077415.3(CRELD1):c.575G>A (p.Cys192Tyr)	rs201866563	0.00014
NM_001077415.3(CRELD1):c.911T>C (p.Leu304Pro)

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