List of variants in gene CARD11 reported as uncertain significance by Blueprint Genetics

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_032415.7(CARD11):c.3145-3C>T	rs200456391	0.00077
NM_032415.7(CARD11):c.1373T>G (p.Ile458Ser)	rs145049015	0.00022
NM_032415.7(CARD11):c.1595C>T (p.Thr532Met)	rs201780608	0.00021
NM_032415.7(CARD11):c.2921G>A (p.Arg974His)	rs750407488	0.00011
NM_032415.7(CARD11):c.3095A>G (p.Asn1032Ser)	rs759214987	0.00003
NM_032415.7(CARD11):c.2608-8C>T	rs1467901142	0.00001
NM_032415.7(CARD11):c.2909A>G (p.Tyr970Cys)	rs1225312452	0.00001
NM_032415.7(CARD11):c.2642G>T (p.Ser881Ile)	rs1583369402
NM_032415.7(CARD11):c.3260+11C>G	rs1583357643
NM_032415.7(CARD11):c.797T>A (p.Val266Asp)	rs1583400791

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