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

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001368894.2(PAX6):c.399+255A>G	rs41275154	0.02233
NM_001368894.2(PAX6):c.369G>A (p.Glu123=)	rs114384476	0.01168
NM_001368894.2(PAX6):c.-129+229G>C	rs577333042	0.01018
NM_001368894.2(PAX6):c.142-149T>A	rs563032643	0.00786
NM_001368894.2(PAX6):c.130C>A (p.Arg44=)	rs141873759	0.00175
NM_001368894.2(PAX6):c.873G>A (p.Gln291=)	rs149053004	0.00075
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.985T>C (p.Leu329=)	rs373147550	0.00024
NM_001368894.2(PAX6):c.-118T>C	rs992201562	0.00016
NM_001368894.2(PAX6):c.807+5C>T	rs376564909	0.00014
NM_001368894.2(PAX6):c.465C>G (p.Gly155=)	rs139803630	0.00009
NM_001368894.2(PAX6):c.11-12C>G	rs766046559	0.00008
NM_001368894.2(PAX6):c.958+4A>T	rs765926181	0.00008
NM_001368894.2(PAX6):c.537G>C (p.Gly179=)	rs374226064	0.00003
NM_001368894.2(PAX6):c.807+6G>A	rs375134684	0.00003
NM_001368894.2(PAX6):c.400-7T>C	rs776848552	0.00001
NM_001368894.2(PAX6):c.435T>C (p.Ala145=)	rs374436481	0.00001
NM_001368894.2(PAX6):c.501C>T (p.Thr167=)	rs201200280	0.00001
NM_001368894.2(PAX6):c.117G>C (p.Pro39=)	rs919486001
NM_001368894.2(PAX6):c.142-142dup	rs202204811
NM_001368894.2(PAX6):c.400-15_400-5del	rs758179195
NM_001368894.2(PAX6):c.561G>T (p.Thr187=)	rs771257263
NM_001368894.2(PAX6):c.724+152TG[27]	rs10525266

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