List of variants in gene CP reported as benign by Illumina Laboratory Services, Illumina

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000096.4(CP):c.2662-12T>C	rs16861582	0.33387
NM_000096.4(CP):c.2286-15del	rs143522213	0.30978
NM_000096.4(CP):c.782-14C>T	rs34067682	0.05131
NM_000096.4(CP):c.1950A>C (p.Gly650=)	rs1053709	0.04222
NM_000096.4(CP):c.1652C>T (p.Thr551Ile)	rs61733458	0.02154
NM_000096.4(CP):c.2286-12T>G	rs183671127	0.01016
NM_000096.4(CP):c.669G>C (p.Val223=)	rs35438054	0.00599
NM_000096.4(CP):c.1275T>C (p.Tyr425=)	rs34237139	0.00484
NM_000096.4(CP):c.1349-13T>C	rs17847017	0.00469
NM_000096.4(CP):c.1348+9T>C	rs35272481	0.00465
NM_000096.4(CP):c.2525A>G (p.Glu842Gly)	rs149858116	0.00437
NM_000096.4(CP):c.2878+12T>G	rs35848147	0.00288
NM_000096.4(CP):c.347C>A (p.Pro116His)	rs73866999	0.00150
NM_000096.4(CP):c.2286-15G>T	rs34861155
NM_000096.4(CP):c.2554+14C>G	rs200965170

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