List of variants in gene TBC1D24 reported as benign by Illumina Laboratory Services, Illumina

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: 28

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HGVS	dbSNP	gnomAD frequency
NM_001199107.2(TBC1D24):c.*2910A>T	rs4786287	0.42768
NM_001199107.2(TBC1D24):c.*188C>T	rs62040717	0.06494
NM_001199107.2(TBC1D24):c.207T>C (p.Pro69=)	rs13339237	0.06245
NM_001199107.2(TBC1D24):c.-31T>C	rs13339105	0.06095
NM_001199107.2(TBC1D24):c.*3715C>T	rs55778555	0.04830
NM_001199107.2(TBC1D24):c.*56C>T	rs76267944	0.03630
NM_001199107.2(TBC1D24):c.*1160G>A	rs7201970	0.02713
NM_001199107.2(TBC1D24):c.1440G>A (p.Ser480=)	rs12373107	0.02286
NM_001199107.2(TBC1D24):c.*1575C>T	rs4786286	0.02254
NM_001199107.2(TBC1D24):c.*2529A>T	rs565226115	0.02169
NM_001199107.2(TBC1D24):c.*732A>G	rs4075481	0.02161
NM_001199107.2(TBC1D24):c.*1814G>C	rs28668740	0.02123
NM_001199107.2(TBC1D24):c.*836C>T	rs4075480	0.02118
NM_001199107.2(TBC1D24):c.1143-6C>T	rs73490287	0.02047
NM_001199107.2(TBC1D24):c.*2395A>G	rs11543247	0.01806
NM_001199107.2(TBC1D24):c.*1691G>A	rs77858505	0.01614
NM_001199107.2(TBC1D24):c.*3712C>T	rs185371000	0.01568
NM_001199107.2(TBC1D24):c.1509C>T (p.Ser503=)	rs189089167	0.01110
NM_001199107.2(TBC1D24):c.*4479C>T	rs1135527	0.00946
NM_001199107.2(TBC1D24):c.*3408C>T	rs9935554	0.00642
NM_001199107.2(TBC1D24):c.*1659G>A	rs115543208	0.00621
NM_001199107.2(TBC1D24):c.*389C>A	rs189378766	0.00596
NM_001199107.2(TBC1D24):c.*4120T>C	rs116622328	0.00448
NM_001199107.2(TBC1D24):c.*385C>T	rs185077219	0.00083
NM_001199107.2(TBC1D24):c.*2598G>C	rs13336179
NM_001199107.2(TBC1D24):c.*2625dup	rs35944492
NM_001199107.2(TBC1D24):c.*36G>T	rs73490289
NM_001199107.2(TBC1D24):c.*4067C>T	rs74003014

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