List of variants in gene TTC21B reported as uncertain significance by Gharavi Laboratory, Columbia University

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024753.5(TTC21B):c.2913dup (p.Val972fs)	rs867205119	0.00005
NM_024753.5(TTC21B):c.1227_1230del (p.Lys410fs)	rs1559066279
NM_024753.5(TTC21B):c.1709C>T (p.Ala570Val)	rs1559058045
NM_024753.5(TTC21B):c.2078_2087del (p.Lys693fs)	rs1559056530
NM_024753.5(TTC21B):c.3397dup (p.Thr1133fs)	rs1559040678
NM_024753.5(TTC21B):c.489del (p.Ala164fs)	rs1559074956

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