List of variants in gene CELSR3 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001407.3(CELSR3):c.4059G>A (p.Gln1353=)	rs145229058	0.00602
NM_001407.3(CELSR3):c.5310C>T (p.Asn1770=)	rs146204269	0.00061
NM_001407.3(CELSR3):c.7395A>G (p.Leu2465=)	rs144325241	0.00006
NM_001407.3(CELSR3):c.133G>A (p.Gly45Ser)
NM_001407.3(CELSR3):c.6295C>T (p.Arg2099Cys)
NM_001407.3(CELSR3):c.7355G>A (p.Arg2452His)
NM_001407.3(CELSR3):c.8658A>G (p.Arg2886=)	rs151064682
NM_001407.3(CELSR3):c.9193C>T (p.Arg3065Cys)

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