Variants in gene TG with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 17

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HGVS	dbSNP	gnomAD frequency
NM_003235.5(TG):c.199G>A (p.Gly67Ser)	rs116340633	0.00924
NM_003235.5(TG):c.3187C>A (p.Leu1063Met)	rs11992497	0.00903
NM_003235.5(TG):c.3313G>A (p.Val1105Ile)	rs115670342	0.00443
NM_003235.5(TG):c.325A>G (p.Ile109Val)	rs35301433	0.00350
NM_003235.5(TG):c.3129C>T (p.His1043=)	rs112300885	0.00347
NM_003235.5(TG):c.144C>T (p.Tyr48=)	rs114436500	0.00345
NM_003235.5(TG):c.6200-7T>A	rs79724982	0.00240
NM_003235.5(TG):c.7083G>T (p.Ala2361=)	rs116723711	0.00239
NM_003235.5(TG):c.7665C>T (p.Arg2555=)	rs115139074	0.00214
NM_003235.5(TG):c.3583G>A (p.Gly1195Arg)	rs138469414	0.00197
NM_003235.5(TG):c.6646A>G (p.Ile2216Val)	rs138690529	0.00179
NM_003235.5(TG):c.3665C>T (p.Ser1222Leu)	rs12549018	0.00164
NM_003235.5(TG):c.3057C>T (p.Ser1019=)	rs116032324	0.00120
NM_003235.5(TG):c.8026C>T (p.Arg2676Trp)	rs114613744	0.00038
NM_003235.5(TG):c.2762-4del
NM_003235.5(TG):c.478+15G>A	rs141561325
NM_003235.5(TG):c.6933T>C (p.Ser2311=)

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