List of variants in gene TTC21B reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_024753.5(TTC21B):c.826A>G (p.Thr276Ala)	rs7592429	0.95088
NM_024753.5(TTC21B):c.601G>A (p.Val201Met)	rs1432273	0.61903
NM_024753.5(TTC21B):c.1695C>T (p.Tyr565=)	rs6750044	0.34586
NM_024753.5(TTC21B):c.2175T>C (p.Phe725=)	rs10176588	0.33260
NM_024753.5(TTC21B):c.1417C>T (p.Leu473Phe)	rs2163649	0.01776
NM_024753.5(TTC21B):c.2334C>T (p.Tyr778=)	rs79656636	0.01606
NM_024753.5(TTC21B):c.1387C>T (p.Pro463Ser)	rs16851307	0.01408
NM_024753.5(TTC21B):c.2385G>C (p.Leu795=)	rs80225158	0.01377
NM_024753.5(TTC21B):c.665A>T (p.Gln222Leu)	rs80026831	0.01296
NM_024753.5(TTC21B):c.838A>G (p.Met280Val)	rs112868646	0.01295
NM_024753.5(TTC21B):c.2742C>T (p.Cys914=)	rs73018799	0.01072
NM_024753.5(TTC21B):c.1867T>C (p.Leu623=)	rs140107312	0.00129
NM_024753.5(TTC21B):c.2472G>A (p.Leu824=)	rs114725374	0.00107
NM_024753.5(TTC21B):c.114C>G (p.Val38=)	rs34486024
NM_024753.5(TTC21B):c.3519T>C (p.Thr1173=)	rs115504901

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