List of variants in gene CNGA3 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001298.3(CNGA3):c.198C>T (p.Thr66=)	rs139544302	0.00147
NM_001298.3(CNGA3):c.1627G>A (p.Asp543Asn)	rs150759499	0.00119
NM_001298.3(CNGA3):c.566+6C>T	rs199558955	0.00080
NM_001298.3(CNGA3):c.1101T>C (p.Gly367=)	rs200069389	0.00034
NM_001298.3(CNGA3):c.1116C>T (p.Pro372=)	rs201649850	0.00031
NM_001298.3(CNGA3):c.210C>T (p.Ile70=)	rs145057274	0.00031
NM_001298.3(CNGA3):c.1413C>T (p.Asn471=)	rs771835849	0.00003
NM_001298.3(CNGA3):c.395+9C>T	rs375494943	0.00003
NM_001298.3(CNGA3):c.1641C>T (p.Phe547=)	rs104893617
NM_001298.3(CNGA3):c.2076A>G (p.Lys692=)
NM_001298.3(CNGA3):c.566+7G>A	rs374306710

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