List of variants in gene TGDS reported as uncertain significance 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_014305.4(TGDS):c.286C>A (p.Leu96Ile)	rs754214510	0.00001
NM_014305.4(TGDS):c.1034T>C (p.Leu345Ser)	rs2139509772
NM_014305.4(TGDS):c.180T>A (p.Asn60Lys)	rs764401457
NM_014305.4(TGDS):c.270_271del (p.Lys91fs)	rs727502809
NM_014305.4(TGDS):c.308A>T (p.His103Leu)	rs147139240
NM_014305.4(TGDS):c.329G>C (p.Arg110Pro)
NM_014305.4(TGDS):c.476C>G (p.Pro159Arg)
NM_014305.4(TGDS):c.582T>G (p.Ser194Arg)	rs2139519010

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