List of variants in gene ARFGEF2 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_006420.3(ARFGEF2):c.1888G>A (p.Val630Ile)	rs146772848	0.00107
NM_006420.3(ARFGEF2):c.3275G>A (p.Arg1092His)	rs151045115	0.00052
NM_006420.3(ARFGEF2):c.5228T>C (p.Met1743Thr)	rs367994107	0.00043
NM_006420.3(ARFGEF2):c.5063C>T (p.Thr1688Ile)	rs145439001	0.00041
NM_006420.3(ARFGEF2):c.4346A>C (p.Asn1449Thr)	rs200473895	0.00026
NM_006420.3(ARFGEF2):c.2973+5G>A	rs759306352	0.00004
NM_006420.3(ARFGEF2):c.5024G>A (p.Arg1675His)	rs778607741	0.00004
NM_006420.3(ARFGEF2):c.2456A>G (p.Tyr819Cys)	rs1047816435	0.00001
NM_006420.3(ARFGEF2):c.3775C>T (p.His1259Tyr)	rs2123521387
NM_006420.3(ARFGEF2):c.3946A>G (p.Met1316Val)	rs1342370443
NM_006420.3(ARFGEF2):c.4832T>C (p.Leu1611Pro)

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