List of variants in gene CRADD reported as likely benign 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_003805.5(CRADD):c.298+59159A>G	rs114077479	0.00245
NM_003805.5(CRADD):c.597G>A (p.Glu199=)	rs116316289	0.00196
NM_003805.5(CRADD):c.546C>T (p.Asn182=)	rs544159440	0.00004
NM_003805.5(CRADD):c.151C>A (p.Leu51Ile)	rs4332566
NM_003805.5(CRADD):c.298+59132A>G

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