List of variants in gene KIF1B reported as benign by PreventionGenetics, part of Exact Sciences

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001365951.3(KIF1B):c.1777+10C>T	rs3753037	0.26503
NM_001365951.3(KIF1B):c.720+17C>T	rs1339458	0.25792
NM_001365951.3(KIF1B):c.285C>G (p.Ala95=)	rs12402052	0.24010
NM_001365951.3(KIF1B):c.5301C>A (p.Thr1767=)	rs11121552	0.23676
NM_001365951.3(KIF1B):c.4299A>G (p.Pro1433=)	rs12125492	0.08850
NM_001365951.3(KIF1B):c.1180+18C>T	rs41274456	0.03074
NM_001365951.3(KIF1B):c.2115+6207G>A	rs75760005	0.02849
NM_001365951.3(KIF1B):c.608+8dup	rs139613776	0.01962
NM_001365951.3(KIF1B):c.363+6A>C	rs114084418	0.01751
NM_001365951.3(KIF1B):c.4798G>A (p.Val1600Met)	rs77172218	0.01096
NM_001365951.3(KIF1B):c.2115+6956A>G	rs148481786	0.00525
NM_001365951.3(KIF1B):c.4158G>A (p.Ser1386=)	rs116302604	0.00481
NM_001365951.3(KIF1B):c.2970C>A (p.Ile990=)	rs78611156	0.00200
NM_001365951.3(KIF1B):c.*2T>C	rs148690591	0.00185
NM_001365951.3(KIF1B):c.184-6_184-5del	rs138324955
NM_001365951.3(KIF1B):c.865-4G>T

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