ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_006420.3(ARFGEF2):c.3663T>C (p.Gly1221=) rs2295580 0.38170
NM_006420.3(ARFGEF2):c.4131C>T (p.Ile1377=) rs2281582 0.13125
NM_006420.3(ARFGEF2):c.169C>T (p.Pro57Ser) rs73113975 0.00540
NM_006420.3(ARFGEF2):c.811C>G (p.Pro271Ala) rs143570842 0.00102
NM_006420.3(ARFGEF2):c.1644G>A (p.Glu548=) rs147534008 0.00098
NM_006420.3(ARFGEF2):c.2686-9C>T rs200945599 0.00092
NM_006420.3(ARFGEF2):c.3456T>C (p.Asp1152=) rs145545997 0.00040
NM_006420.3(ARFGEF2):c.2940C>T (p.Thr980=) rs41296217 0.00031
NM_006420.3(ARFGEF2):c.756C>T (p.Asn252=) rs114729625 0.00031
NM_006420.3(ARFGEF2):c.4812G>A (p.Lys1604=) rs142036030 0.00014
NM_006420.3(ARFGEF2):c.2640G>A (p.Pro880=) rs368844677 0.00013
NM_006420.3(ARFGEF2):c.1953C>T (p.Ile651=) rs377322572 0.00011
NM_006420.3(ARFGEF2):c.3003C>T (p.Leu1001=) rs752737205 0.00006
NM_006420.3(ARFGEF2):c.3120C>T (p.Leu1040=) rs751240187 0.00006
NM_006420.3(ARFGEF2):c.1017G>C (p.Gly339=) rs765982548 0.00005
NM_006420.3(ARFGEF2):c.4320T>C (p.Asn1440=) rs758848307 0.00002
NM_006420.3(ARFGEF2):c.1203G>A (p.Leu401=) rs747567218 0.00001
NM_006420.3(ARFGEF2):c.2412C>T (p.Ile804=) rs750860901 0.00001
NM_006420.3(ARFGEF2):c.4749C>T (p.Ala1583=) rs757878455 0.00001
NM_006420.3(ARFGEF2):c.1014C>T (p.Asn338=) rs201523904

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