List of variants in gene ARFGEF2 reported as benign by Genetic Services Laboratory, University of Chicago

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_006420.3(ARFGEF2):c.423+3A>G	rs2295029	0.00491
NM_006420.3(ARFGEF2):c.1512G>A (p.Thr504=)	rs116550473	0.00395
NM_006420.3(ARFGEF2):c.807C>T (p.Asp269=)	rs149172723	0.00230
NM_006420.3(ARFGEF2):c.1275C>T (p.His425=)	rs117131028	0.00143
NM_006420.3(ARFGEF2):c.1398T>C (p.Phe466=)	rs141596938	0.00081
NM_006420.3(ARFGEF2):c.3177G>A (p.Ser1059=)	rs61748373

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