List of variants in gene ARFGEF2 reported as benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_006420.3(ARFGEF2):c.839-20A>G	rs2295031	0.38231
NM_006420.3(ARFGEF2):c.3663T>C (p.Gly1221=)	rs2295580	0.38170
NM_006420.3(ARFGEF2):c.4755+19A>G	rs7270848	0.36848
NM_006420.3(ARFGEF2):c.2277-16G>A	rs4810905	0.23578
NM_006420.3(ARFGEF2):c.4131C>T (p.Ile1377=)	rs2281582	0.13125
NM_006420.3(ARFGEF2):c.424-16C>T	rs41304647	0.04427
NM_006420.3(ARFGEF2):c.1425+11C>T	rs74970217	0.00818
NM_006420.3(ARFGEF2):c.169C>T (p.Pro57Ser)	rs73113975	0.00540
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.2815-7G>A	rs187176143	0.00034
NM_006420.3(ARFGEF2):c.3177G>A (p.Ser1059=)	rs61748373

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