List of variants in gene GLI2 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001374353.1(GLI2):c.457+70G>A	rs11681136	0.93205
NM_001374353.1(GLI2):c.3865G>A (p.Asp1289Asn)	rs12711538	0.66550
NM_001374353.1(GLI2):c.3888A>G (p.Pro1296=)	rs10167980	0.61468
NM_001374353.1(GLI2):c.1893C>T (p.Thr631=)	rs13008360	0.02306
NM_001374353.1(GLI2):c.1633-17C>T	rs78949549	0.01801
NM_001374353.1(GLI2):c.963C>G (p.Pro321=)	rs149894186	0.01440
NM_001374353.1(GLI2):c.1710G>A (p.Thr570=)	rs61732852	0.01154
NM_001374353.1(GLI2):c.1818C>A (p.Gly606=)	rs61732850	0.00832
NM_001374353.1(GLI2):c.3539G>A (p.Gly1180Asp)	rs114823319	0.00522
NM_001374353.1(GLI2):c.720C>T (p.Asp240=)	rs142793481	0.00483
NM_001374353.1(GLI2):c.4281G>A (p.Met1427Ile)	rs146467786	0.00465
NM_001374353.1(GLI2):c.4282C>T (p.Leu1428Phe)	rs146207623	0.00465
NM_001374353.1(GLI2):c.1935G>A (p.Ser645=)	rs114259687	0.00177
NM_001374353.1(GLI2):c.4281_4282delinsAT (p.Met1427_Leu1428delinsIlePhe)	rs1553479775

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