List of variants in gene CELSR1 reported as likely pathogenic for immune system disorder

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_001378328.1(CELSR1):c.2042del (p.Asn681fs)	rs1569226110
NM_001378328.1(CELSR1):c.5512C>T (p.Arg1838Ter)
NM_001378328.1(CELSR1):c.5702-1G>C	rs1569133268
NM_001378328.1(CELSR1):c.868G>T (p.Glu290Ter)	rs1569227576

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