ClinVar Miner

List of variants reported as pathogenic for color vision disorder by DBGen Ocular Genomics

Included ClinVar conditions (16):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000513.2(OPN1MW):c.807_948del (p.Met269fs)	rs2148787747
NM_001298.3(CNGA3):c.1519del (p.Asp507fs)	rs745592705
NM_006204.4(PDE6C):c.480G>T (p.Lys160Asn)	rs765296989

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