List of variants in gene GLI3 reported as uncertain significance 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000168.6(GLI3):c.2119C>T (p.Pro707Ser)	rs121917716	0.00028
NM_000168.6(GLI3):c.1028+3A>T	rs368499795	0.00021
NM_000168.6(GLI3):c.313C>T (p.Arg105Cys)	rs555794809	0.00003
NM_000168.6(GLI3):c.507G>A (p.Pro169=)	rs759525362	0.00003
NM_000168.6(GLI3):c.1593T>C (p.Tyr531=)	rs749798195	0.00002
GRCh37/hg19 7p14.1(chr7:41942712-42378563)x3
NM_000168.6(GLI3):c.3098C>A (p.Pro1033Gln)	rs376956433
NM_000168.6(GLI3):c.3140_3141delinsCA (p.Gln1047Pro)	rs1064796326
NM_000168.6(GLI3):c.3284A>G (p.Asp1095Gly)	rs1554304659
NM_000168.6(GLI3):c.3970G>C (p.Ala1324Pro)	rs1480007692

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