List of variants in gene PAX6 reported as likely benign for retinal disorder

Minimum submission review status:		Collection method:
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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: 5

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HGVS	dbSNP	gnomAD frequency
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.-180A>G	rs75563367	0.00766
NM_001368894.2(PAX6):c.972A>T (p.Thr324=)	rs779631884	0.00001
NM_001368894.2(PAX6):c.1221A>C (p.Ser407=)	rs1949622831

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