List of variants in gene combination KIF1B, LOC129388447 reported as uncertain significance for embryonal neoplasm

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001365951.3(KIF1B):c.364-15A>G	rs771929965	0.00002
NM_001365951.3(KIF1B):c.364-10A>G	rs886044966	0.00001

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