List of variants in gene PAX6 reported as likely benign for not specified

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001368894.2(PAX6):c.1032G>A (p.Pro344=)	rs146261351	0.00048
NM_001368894.2(PAX6):c.465C>G (p.Gly155=)	rs139803630	0.00009
NM_001368894.2(PAX6):c.1215C>T (p.Thr405=)	rs886038486	0.00001
NM_000280.4(PAX6):c.-125dup
NM_001368894.2(PAX6):c.-117dup	rs1554986858
NM_001368894.2(PAX6):c.724+14T>A

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