List of variants in gene PAX6 reported as benign for corneal disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001368894.2(PAX6):c.808-12C>T	rs667773	0.05916
NM_001368894.2(PAX6):c.-129+9G>A	rs56139994	0.02711
NM_001368894.2(PAX6):c.369G>A (p.Glu123=)	rs114384476	0.01168
NM_001368894.2(PAX6):c.1075-275A>C	rs3026392	0.00180
NM_001368894.2(PAX6):c.130C>A (p.Arg44=)	rs141873759	0.00175
NM_001368894.2(PAX6):c.-107C>T	rs111270711	0.00117
NM_001368894.2(PAX6):c.873G>A (p.Gln291=)	rs149053004	0.00075
NM_001368894.2(PAX6):c.1032G>A (p.Pro344=)	rs146261351	0.00048
NM_001368894.2(PAX6):c.1179A>C (p.Thr393=)	rs143477661	0.00038
NM_001368894.2(PAX6):c.753G>A (p.Val251=)	rs145329506	0.00038
NM_001368894.2(PAX6):c.978C>T (p.Gly326=)	rs115833025	0.00035
NM_001368894.2(PAX6):c.909T>C (p.Ser303=)	rs202154006	0.00004
NM_001368894.2(PAX6):c.1166C>A (p.Pro389Gln)	rs200015827	0.00003
NM_001368894.2(PAX6):c.959-7C>T	rs750093295	0.00003
NM_001368894.2(PAX6):c.243A>G (p.Arg81=)	rs771974160	0.00001
NM_001368894.2(PAX6):c.724+14del	rs772158967

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