List of variants in gene FGA reported 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
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_021871.4(FGA):c.991A>G (p.Thr331Ala)	rs6050	0.29452
NM_021871.4(FGA):c.510+1G>T	rs146387238	0.00009
NM_000508.3(FGA):c.103C>T (p.Arg35Cys)	rs121909606	0.00001
NM_000508.3(FGA):c.112A>G (p.Arg38Gly)	rs121909608	0.00001
NM_000508.3(FGA):c.92G>T (p.Gly31Val)	rs121909605	0.00001
NM_021871.4(FGA):c.104G>A (p.Arg35His)	rs121909607	0.00001
NM_021871.4(FGA):c.1634A>T (p.Glu545Val)	rs121909612	0.00001
NM_000508.3(FGA):c.1358G>A (p.Ser453Asn)	rs121909610
NM_021871.4(FGA):c.1037del (p.Asn346fs)
NM_021871.4(FGA):c.1055del (p.Pro352fs)	rs1299596156
NM_021871.4(FGA):c.1121C>A (p.Thr374Asn)
NM_021871.4(FGA):c.1452del (p.Ser485fs)	rs2530820376
NM_021871.4(FGA):c.1456G>A (p.Glu486Lys)
NM_021871.4(FGA):c.163T>C (p.Cys55Arg)	rs2530829969
NM_021871.4(FGA):c.1736dup (p.Tyr579Ter)
NM_021871.4(FGA):c.368G>A (p.Arg123His)
NM_021871.4(FGA):c.389T>C (p.Val130Ala)
NM_021871.4(FGA):c.55-1G>T

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