List of variants in gene CRPPA reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001101426.4(CRPPA):c.808C>T (p.Leu270Phe)	rs200334999	0.00045
NM_001101426.4(CRPPA):c.226C>G (p.Leu76Val)	rs939213590	0.00006
NM_001101426.4(CRPPA):c.1234C>G (p.Leu412Val)	rs747967711	0.00001
NM_001101426.4(CRPPA):c.979C>G (p.Leu327Val)	rs587780361

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