List of variants in gene combination KIF1B, LOC129388447 reported as uncertain significance for Charcot-Marie-Tooth disease type 2

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001365951.3(KIF1B):c.391A>G (p.Asn131Asp)	rs770849620	0.00001
NM_001365951.3(KIF1B):c.392A>G (p.Asn131Ser)	rs776533873	0.00001
NM_001365951.3(KIF1B):c.399C>G (p.Asn133Lys)	rs996589396
NM_001365951.3(KIF1B):c.400T>C (p.Cys134Arg)
NM_001365951.3(KIF1B):c.415T>G (p.Ser139Ala)
NM_001365951.3(KIF1B):c.422C>G (p.Ser141Cys)	rs2102194265

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