ClinVar Miner

List of variants in gene CARD14 reported as likely pathogenic for not provided

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001366385.1(CARD14):c.681T>G (p.Tyr227Ter)	rs369755459	0.00006
NM_001366385.1(CARD14):c.467T>C (p.Leu156Pro)	rs387907240

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