Variants in gene CRPPA with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001101426.4(CRPPA):c.726A>G (p.Gln242=)	rs61746966	0.02747
NM_001101426.4(CRPPA):c.407C>T (p.Ala136Val)	rs61734789	0.02478
NM_001101426.4(CRPPA):c.947C>A (p.Thr316Lys)	rs114363936	0.00703
NM_001101426.4(CRPPA):c.346C>T (p.Arg116Cys)	rs61744487	0.00561
NM_001101426.4(CRPPA):c.*86A>G	rs16878685	0.00522
NM_001101426.4(CRPPA):c.1220T>C (p.Leu407Ser)	rs141625803	0.00198
NM_001101426.4(CRPPA):c.1059G>A (p.Lys353=)	rs181099904	0.00151
NM_001101426.4(CRPPA):c.790-14T>C	rs142414812	0.00123
NM_001101426.4(CRPPA):c.*73TG[5]	rs139003391
NM_001101426.4(CRPPA):c.685-25GTT[6]	rs142647500
NM_001101426.4(CRPPA):c.836-9del	rs3839757

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