List of variants in gene TTBK2 reported as benign by GeneDx

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_173500.4(TTBK2):c.1197+86G>A	rs9920092	0.78475
NM_173500.4(TTBK2):c.23T>C (p.Leu8Pro)	rs6493068	0.46763
NM_173500.4(TTBK2):c.538-90G>A	rs7182753	0.46022
NM_173500.4(TTBK2):c.-67-138A>G	rs8036096	0.46016
NM_173500.4(TTBK2):c.1409+215G>A	rs11854550	0.20530
NM_173500.4(TTBK2):c.603+87A>T	rs7183673	0.14313
NM_173500.4(TTBK2):c.822+219G>A	rs11853250	0.13864
NM_173500.4(TTBK2):c.538-184A>T	rs34920950	0.12954
NM_173500.4(TTBK2):c.603+89del	rs66534174	0.12662
NM_173500.4(TTBK2):c.603+87del	rs66947001	0.12463
NM_173500.4(TTBK2):c.69+123C>T	rs62020680	0.09975
NM_173500.4(TTBK2):c.-8G>A	rs16957250	0.08842
NM_173500.4(TTBK2):c.696+121G>A	rs8032994	0.06536
NM_173500.4(TTBK2):c.3272+145C>G	rs73410971	0.06381
NM_173500.4(TTBK2):c.3272+117T>C	rs73410972	0.06118
NM_173500.4(TTBK2):c.1410-153A>G	rs117242112	0.05105
NM_173500.4(TTBK2):c.-67-240T>A	rs8034933	0.03745
NM_173500.4(TTBK2):c.3251C>T (p.Thr1084Met)	rs34348991	0.02971
NM_173500.4(TTBK2):c.292-212G>A	rs150735909	0.02424
NM_173500.4(TTBK2):c.3273-36A>G	rs116718595	0.00576
NM_173500.4(TTBK2):c.937A>G (p.Thr313Ala)	rs56017612	0.00359
NM_173500.4(TTBK2):c.538-185del	rs367546137
NM_173500.4(TTBK2):c.69+21GT[19]	rs10650948
NM_173500.4(TTBK2):c.69+21GT[20]	rs10650948
NM_173500.4(TTBK2):c.980+105C>A	rs16957167
NM_173500.4(TTBK2):c.981-124dup	rs34530003

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