List of variants in gene PAX6 reported as likely pathogenic for carcinoma

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000280.4:c.1267A>T
NM_001368894.2(PAX6):c.112C>G (p.Arg38Gly)	rs397514640
NM_001368894.2(PAX6):c.256G>C (p.Gly86Arg)	rs759557055
NM_001368894.2(PAX6):c.400G>A (p.Val134Met)

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