List of variants in gene STIL 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001048166.1(STIL):c.3486T>C (p.Pro1162=)	rs2758735	0.41846
NM_001048166.1(STIL):c.2954A>G (p.His985Arg)	rs13376679	0.25624
NM_001048166.1(STIL):c.3378A>G (p.Arg1126=)	rs142315727	0.00478
NM_001048166.1(STIL):c.3786G>A (p.Thr1262=)	rs146387723	0.00460
NM_001048166.1(STIL):c.1055G>A (p.Arg352His)	rs141678367	0.00323
NM_001048166.1(STIL):c.1136C>T (p.Ser379Phe)	rs149185431	0.00258

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