List of variants in gene KBTBD13 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001101362.3(KBTBD13):c.212C>A (p.Ala71Glu)	rs759104102
NM_001101362.3(KBTBD13):c.477del (p.Ala159_Val160insTer)	rs1555407608
NM_001101362.3(KBTBD13):c.496G>C (p.Ala166Pro)	rs777916743

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