List of variants in gene PRKAR1A reported as uncertain significance for cardiovascular disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_002734.5(PRKAR1A):c.1024C>T (p.Arg342Cys)	rs146383819	0.00006
NM_002734.5(PRKAR1A):c.549+20A>G	rs981055703	0.00004
NM_002734.5(PRKAR1A):c.1025G>A (p.Arg342His)	rs760033566	0.00001
NM_002734.5(PRKAR1A):c.25A>G (p.Ser9Gly)	rs778468626
NM_002734.5(PRKAR1A):c.424GAT[1] (p.Asp143del)	rs1308936763
NM_002734.5(PRKAR1A):c.464C>T (p.Ser155Leu)	rs1568696484
NM_002734.5(PRKAR1A):c.550G>A (p.Val184Ile)	rs773162575
NM_002734.5(PRKAR1A):c.691T>C (p.Tyr231His)	rs2143324114
NM_002734.5(PRKAR1A):c.797C>T (p.Thr266Met)	rs1329426125

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