List of variants in gene CDH15 reported as 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004933.3(CDH15):c.2025G>A (p.Pro675=)	rs62068507	0.00683
NM_004933.3(CDH15):c.598G>A (p.Glu200Lys)	rs141084668	0.00098
NM_004933.3(CDH15):c.131G>A (p.Arg44Gln)	rs199879102	0.00011
NM_004933.3(CDH15):c.1666C>T (p.Arg556Cys)
NM_004933.3(CDH15):c.2054C>T (p.Pro685Leu)
NM_004933.3(CDH15):c.2137G>A (p.Asp713Asn)

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