Variants in gene PRKAR1A with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_002734.5(PRKAR1A):c.221G>A (p.Arg74His)	rs200069356	0.00036
NM_002734.5(PRKAR1A):c.103A>G (p.Ile35Val)	rs377513504	0.00009
NM_002734.5(PRKAR1A):c.19G>A (p.Ala7Thr)	rs369210646	0.00003
NM_002734.5(PRKAR1A):c.-11C>T	rs1021510770	0.00001
NM_002734.5(PRKAR1A):c.309G>A (p.Glu103=)	rs746113372	0.00001
NM_002734.5(PRKAR1A):c.349-5T>C	rs1456043929
NM_002734.5(PRKAR1A):c.441-5del	rs777677808
NM_002734.5(PRKAR1A):c.770-8T>G	rs182841147

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