List of variants in gene CARD11 reported as likely pathogenic by University of Washington Center for Mendelian Genomics, University of Washington

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_032415.7(CARD11):c.128C>T (p.Thr43Met)	rs2115094112
NM_032415.7(CARD11):c.173A>G (p.Asp58Gly)	rs1780506565
NM_032415.7(CARD11):c.179T>A (p.Val60Glu)	rs1583410780
NM_032415.7(CARD11):c.191C>G (p.Pro64Arg)	rs1583410771
NM_032415.7(CARD11):c.215G>T (p.Arg72Leu)	rs2115093887
NM_032415.7(CARD11):c.220+1G>A	rs1554276623
NM_032415.7(CARD11):c.358+1G>A	rs2115090359

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