List of variants in gene CARD14 reported as likely pathogenic for exanthem

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001366385.1(CARD14):c.356T>C (p.Met119Thr)	rs1598639584
NM_001366385.1(CARD14):c.371T>C (p.Leu124Pro)	rs1598639617
NM_001366385.1(CARD14):c.409GAG[1] (p.Glu138del)	rs1390003312

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