List of variants in gene CARD14 reported as likely benign by GeneDx

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001366385.1(CARD14):c.963+193C>T	rs62074374	0.03681
NM_001366385.1(CARD14):c.1090-115G>A	rs55775426	0.03566
NM_001366385.1(CARD14):c.1170C>T (p.Phe390=)	rs74951924	0.03377
NM_001366385.1(CARD14):c.1264G>A (p.Glu422Lys)	rs61751629	0.02212
NM_001366385.1(CARD14):c.349+322C>T	rs115120883	0.01542
NM_001366385.1(CARD14):c.676-269G>A	rs8070632	0.01509
NM_001366385.1(CARD14):c.844-122G>A	rs149842500	0.01243
NM_001366385.1(CARD14):c.675+255G>T	rs117087009	0.01155
NM_001366385.1(CARD14):c.676-248C>T	rs114702862	0.01093
NM_001366385.1(CARD14):c.1357-175G>A	rs117253827	0.00984
NM_001366385.1(CARD14):c.1476C>T (p.Phe492=)	rs144710573	0.00465
NM_001366385.1(CARD14):c.1851+350C>A	rs181610887	0.00033
NM_001366385.1(CARD14):c.1371G>A (p.Ser457=)	rs62074378

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