ClinVar Miner

List of variants in gene combination CARD14, SGSH reported by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001366385.1(CARD14):c.2871G>C (p.Glu957Asp)	rs373510767	0.00006
NM_001366385.1(CARD14):c.2007G>A (p.Glu669=)	rs2510722046

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