List of variants in gene CRPPA reported as benign for not specified

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001101426.4(CRPPA):c.534+13T>A	rs6461252	0.47530
NM_001101426.4(CRPPA):c.1026+45_1026+46del	rs139478143	0.08746
NM_001101426.4(CRPPA):c.726A>G (p.Gln242=)	rs61746966	0.02927
NM_001101426.4(CRPPA):c.1251+50A>G	rs78374272	0.02578
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.1251+18C>T	rs201599524	0.00339
NM_001101426.4(CRPPA):c.1220T>C (p.Leu407Ser)	rs141625803	0.00164
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.*34C>G	rs16878689
NM_001101426.4(CRPPA):c.685-25GTT[6]	rs142647500
NM_001101426.4(CRPPA):c.836-19dup	rs3839757

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