List of variants in gene combination IFT80, TRIM59-IFT80 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_020800.3(IFT80):c.1756A>T (p.Thr586Ser)	rs6778728	0.31629
NM_020800.3(IFT80):c.1926+13T>C	rs3737214	0.17528
NM_020800.3(IFT80):c.*42G>A	rs16831149	0.15568
NM_020800.3(IFT80):c.462G>A (p.Ala154=)	rs34182424	0.02371
NM_020800.3(IFT80):c.-40C>T	rs79756374	0.01997
NM_020800.3(IFT80):c.1076C>T (p.Ser359Phe)	rs144099135	0.00742
NM_020800.3(IFT80):c.*1204G>A	rs144132950	0.00376

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