List of variants in gene CEL reported as uncertain significance 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001807.6(CEL):c.1966G>C (p.Ala656Pro)	rs587780309	0.00172
NM_001807.6(CEL):c.2172del (p.Val725fs)	rs780419796	0.00115
NM_001807.6(CEL):c.347G>A (p.Arg116Gln)	rs199675811	0.00036
NM_001807.6(CEL):c.878C>T (p.Pro293Leu)	rs201066180	0.00020
NM_001807.6(CEL):c.998T>C (p.Ile333Thr)	rs368511384	0.00004
NM_001807.6(CEL):c.1333C>G (p.Pro445Ala)	rs751702926	0.00002
NM_001807.6(CEL):c.400G>A (p.Gly134Ser)	rs377284693	0.00002
NM_001807.6(CEL):c.178A>G (p.Lys60Glu)	rs1433124386	0.00001
NM_001807.6(CEL):c.979G>A (p.Ala327Thr)	rs751119069	0.00001
NM_001807.6(CEL):c.-13G>A	rs2119054429
NM_001807.6(CEL):c.1974del (p.Val659fs)	rs1341981506
NM_001807.6(CEL):c.687C>T (p.Asn229=)	rs1554732495

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