List of variants in gene GLI2 reported as benign by Eurofins NTD LLC (GA)

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: 23

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HGVS	dbSNP	gnomAD frequency
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.3415G>T (p.Ala1139Ser)	rs3738880	0.61025
NM_001374353.1(GLI2):c.2889C>T (p.Ser963=)	rs146811565	0.04735
NM_001374353.1(GLI2):c.2997C>T (p.Asp999=)	rs140479803	0.02616
NM_001374353.1(GLI2):c.3892C>T (p.Pro1298Ser)	rs114376238	0.01651
NM_001374353.1(GLI2):c.4003A>G (p.Met1335Val)	rs149140724	0.00970
NM_001374353.1(GLI2):c.4507G>A (p.Asp1503Asn)	rs114814747	0.00964
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.4612T>C (p.Ser1538Pro)	rs144372453	0.00352
NM_001374353.1(GLI2):c.2037A>G (p.Ala679=)	rs146059306	0.00325
NM_001374353.1(GLI2):c.2967C>T (p.Gly989=)	rs373880077	0.00285
NM_001374353.1(GLI2):c.3298G>T (p.Val1100Leu)	rs147580961	0.00222
NM_001374353.1(GLI2):c.3477G>T (p.Gln1159His)	rs139686081	0.00181
NM_001374353.1(GLI2):c.1935G>A (p.Ser645=)	rs114259687	0.00177
NM_001374353.1(GLI2):c.1243G>A (p.Val415Met)	rs142296407	0.00124
NM_001374353.1(GLI2):c.1808C>T (p.Thr603Met)	rs142775128	0.00099
NM_001374353.1(GLI2):c.4577G>A (p.Arg1526His)	rs138987487	0.00059
NM_001374353.1(GLI2):c.2657C>G (p.Thr886Ser)	rs572826436	0.00001
NM_001374353.1(GLI2):c.2136C>A (p.Phe712Leu)	rs151179617

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