List of variants in gene combination KIF1B, LOC126805614 reported as uncertain significance for peripheral neuropathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 34

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HGVS	dbSNP	gnomAD frequency
NM_001365951.3(KIF1B):c.2827G>A (p.Ala943Thr)	rs142567076	0.00037
NM_001365951.3(KIF1B):c.2824G>A (p.Asp942Asn)	rs370647925	0.00004
NM_001365951.3(KIF1B):c.2693G>A (p.Gly898Asp)	rs766101107	0.00002
NM_001365951.3(KIF1B):c.2744C>T (p.Thr915Met)	rs749523745	0.00002
NM_001365951.3(KIF1B):c.2704G>A (p.Glu902Lys)	rs368663292	0.00001
NM_001365951.3(KIF1B):c.2719C>T (p.Arg907Cys)	rs1334915559	0.00001
NM_001365951.3(KIF1B):c.2749G>A (p.Asp917Asn)	rs768941996	0.00001
NM_001365951.3(KIF1B):c.2818G>A (p.Val940Met)	rs764144206	0.00001
NM_001365951.3(KIF1B):c.2830G>A (p.Gly944Ser)	rs755314640	0.00001
NM_001365951.3(KIF1B):c.2839G>T (p.Ala947Ser)	rs748284088	0.00001
NM_001365951.3(KIF1B):c.2846C>T (p.Thr949Met)	rs141942131	0.00001
NM_001365951.3(KIF1B):c.2676-3T>C
NM_001365951.3(KIF1B):c.2678C>T (p.Ser893Phe)
NM_001365951.3(KIF1B):c.2692G>A (p.Gly898Ser)
NM_001365951.3(KIF1B):c.2696G>A (p.Cys899Tyr)
NM_001365951.3(KIF1B):c.2707C>G (p.Arg903Gly)	rs868254486
NM_001365951.3(KIF1B):c.2708G>C (p.Arg903Pro)	rs778403355
NM_001365951.3(KIF1B):c.2716G>A (p.Asp906Asn)	rs758389718
NM_001365951.3(KIF1B):c.2716G>T (p.Asp906Tyr)
NM_001365951.3(KIF1B):c.2720G>A (p.Arg907His)	rs1651714039
NM_001365951.3(KIF1B):c.2753C>T (p.Ser918Phe)
NM_001365951.3(KIF1B):c.2776G>A (p.Glu926Lys)
NM_001365951.3(KIF1B):c.2786A>T (p.Asp929Val)	rs2102301786
NM_001365951.3(KIF1B):c.2837A>G (p.Asp946Gly)	rs2102301877
NM_001365951.3(KIF1B):c.2854G>C (p.Gly952Arg)
NM_001365951.3(KIF1B):c.2863C>T (p.Leu955Phe)
NM_001365951.3(KIF1B):c.2869A>G (p.Ser957Gly)	rs556117169
NM_001365951.3(KIF1B):c.2875_2883del (p.Gly959_Asp961del)	rs1651722145
NM_001365951.3(KIF1B):c.2876G>T (p.Gly959Val)
NM_001365951.3(KIF1B):c.2885C>T (p.Pro962Leu)	rs762619916
NM_001365951.3(KIF1B):c.2899T>A (p.Ser967Thr)
NM_001365951.3(KIF1B):c.2905T>C (p.Trp969Arg)	rs1569831309
NM_001365951.3(KIF1B):c.2918T>G (p.Val973Gly)
NM_001365951.3(KIF1B):c.2924+5G>A

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