List of variants in gene TTC21B reported as uncertain significance by Eurofins NTD LLC (GA)

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_024753.5(TTC21B):c.2587C>T (p.Arg863Trp)	rs34489989	0.00108
NM_024753.5(TTC21B):c.691A>T (p.Thr231Ser)	rs149925563	0.00071
NM_024753.5(TTC21B):c.1697A>G (p.His566Arg)	rs146320075	0.00063
NM_024753.5(TTC21B):c.3932G>A (p.Arg1311His)	rs139327086	0.00056
NM_024753.5(TTC21B):c.549T>C (p.Gly183=)	rs141664029	0.00014
NM_024753.5(TTC21B):c.796-3T>C	rs794727932	0.00004
NM_024753.5(TTC21B):c.1358T>A (p.Met453Lys)	rs373845234	0.00003
NM_024753.5(TTC21B):c.2168G>A (p.Arg723Gln)	rs151309609	0.00003
NM_024753.5(TTC21B):c.3264-3C>G	rs189122492	0.00003
NM_024753.5(TTC21B):c.1088-3T>C	rs761658519	0.00001
NM_024753.5(TTC21B):c.2530A>G (p.Met844Val)	rs766811699

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