List of variants in gene CP 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000096.4(CP):c.1430C>T (p.Pro477Leu)	rs35331711	0.00242
NM_000096.4(CP):c.322C>T (p.His108Tyr)	rs34386552	0.00235
NM_000096.4(CP):c.2793A>G (p.Leu931=)	rs34987997	0.00186
NM_000096.4(CP):c.2684G>C (p.Gly895Ala)	rs139633388	0.00162
NM_000096.4(CP):c.1960G>A (p.Asp654Asn)	rs755243937	0.00004
NM_000096.4(CP):c.530G>A (p.Arg177Lys)	rs142350562	0.00004
NM_000096.4(CP):c.2500A>G (p.Ile834Val)	rs1377096899	0.00001
NM_000096.4(CP):c.656T>A (p.Val219Glu)	rs587780321	0.00001
NM_000096.4(CP):c.2847T>G (p.Asp949Glu)	rs201431095
NM_000096.4(CP):c.737T>G (p.Val246Gly)	rs797045480

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