List of variants in gene KDR reported as not provided by ITMI

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_002253.4(KDR):c.1416A>T (p.Gln472His)	rs1870377	0.20077
NM_002253.4(KDR):c.889G>A (p.Val297Ile)	rs2305948	0.14032
NM_002253.4(KDR):c.-1G>T	rs56233104	0.03835
NM_002253.4(KDR):c.1444T>C (p.Cys482Arg)	rs34231037	0.02299
NM_002253.4(KDR):c.1987+28C>T	rs17085310	0.01097
NM_002253.4(KDR):c.1116G>C (p.Glu372Asp)	rs113121239	0.00691
NM_002253.4(KDR):c.2066C>T (p.Thr689Met)	rs34038364	0.00307
NM_002253.4(KDR):c.1384T>G (p.Leu462Val)	rs56286620	0.00175
NM_002253.4(KDR):c.1615G>A (p.Gly539Arg)	rs55716939	0.00150
NM_002253.4(KDR):c.170G>C (p.Arg57Thr)	rs139047809	0.00127
NM_002253.4(KDR):c.406G>A (p.Val136Met)	rs35636987	0.00028
NM_002253.4(KDR):c.794C>T (p.Ser265Leu)	rs539911006	0.00009
NM_002253.4(KDR):c.895C>T (p.Arg299Trp)	rs368062574	0.00006
NM_002253.4(KDR):c.1151C>T (p.Thr384Met)	rs201708587	0.00003
NM_002253.4(KDR):c.3439C>T (p.Pro1147Ser)	rs121917766	0.00003
NM_002253.4(KDR):c.3808A>C (p.Lys1270Gln)	rs587778427	0.00003
NM_002253.4(KDR):c.1192G>A (p.Val398Ile)	rs587778430	0.00001
NM_002253.4(KDR):c.1493A>T (p.Glu498Val)	rs587778424	0.00001
NM_002253.4(KDR):c.724C>T (p.Leu242Phe)	rs587778428	0.00001
NM_002253.4(KDR):c.1055C>T (p.Ala352Val)	rs151317075
NM_002253.4(KDR):c.2305G>A (p.Val769Ile)	rs587778425
NM_002253.4(KDR):c.2674A>G (p.Ile892Val)	rs587778426
NM_002253.4(KDR):c.787C>T (p.Pro263Ser)	rs587778429

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