List of variants in gene FGG reported as uncertain significance for coagulation protein disease

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_021870.3(FGG):c.*488C>T	rs191297318	0.00453
NM_021870.3(FGG):c.571G>A (p.Gly191Arg)	rs6063	0.00339
NM_021870.3(FGG):c.*496A>C	rs187316301	0.00268
NM_021870.3(FGG):c.*500C>T	rs183036893	0.00103
NM_021870.3(FGG):c.140C>T (p.Thr47Ile)	rs138511699	0.00050
NM_021870.3(FGG):c.124G>A (p.Gly42Ser)	rs202132393	0.00034
NM_021870.3(FGG):c.318C>T (p.Asp106=)	rs150242757	0.00016
NM_021870.3(FGG):c.1258A>G (p.Ile420Val)	rs374917187	0.00015
NM_021870.3(FGG):c.620A>G (p.Tyr207Cys)	rs775086103	0.00008
NM_021870.3(FGG):c.19C>T (p.Pro7Ser)	rs374845868	0.00006
NM_021870.3(FGG):c.709T>C (p.Tyr237His)	rs762488338	0.00005
NM_021870.3(FGG):c.1285G>T (p.Gly429Trp)	rs145938787	0.00003
NM_021870.3(FGG):c.683T>C (p.Val228Ala)	rs757702704	0.00002
NM_021870.3(FGG):c.*494A>G	rs1731056413	0.00001
NM_021870.3(FGG):c.1125C>T (p.Tyr375=)	rs766524002	0.00001
NM_021870.3(FGG):c.502A>G (p.Thr168Ala)	rs141559764	0.00001
NM_021870.3(FGG):c.667-10G>C	rs886059155	0.00001
NM_000509.5(FGG):c.-53A>G	rs886059156
NM_021870.3(FGG):c.1190C>T (p.Thr397Ile)	rs1731071910
NM_021870.3(FGG):c.1202G>A (p.Arg401Gln)	rs2110838894
NM_021870.3(FGG):c.1237A>G (p.Ile413Val)	rs886059154
NM_021870.3(FGG):c.1300G>T (p.Val434Phe)
NM_021870.3(FGG):c.401G>A (p.Arg134Gln)	rs764559342
NM_021870.3(FGG):c.606G>C (p.Gln202His)	rs2110846559
NM_021870.3(FGG):c.694A>G (p.Lys232Glu)	rs2110844685
NM_021870.3(FGG):c.700T>C (p.Trp234Arg)	rs2110844651
NM_021870.3(FGG):c.793C>T (p.Gln265Ter)	rs771279321

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