ClinVar Miner

List of variants in gene CARD14 reported by Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001366385.1(CARD14):c.675+26G>A	rs4889991	0.77525
NM_001366385.1(CARD14):c.633G>A (p.Glu211=)	rs4889990	0.37893
NM_001366385.1(CARD14):c.1753G>A (p.Val585Ile)	rs34367357	0.06519

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