Variants in gene TRDN with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.1713A>C (p.Glu571Asp)	rs201115952	0.00133
NM_006073.4(TRDN):c.1367A>G (p.Gln456Arg)	rs200243235	0.00128
NM_006073.4(TRDN):c.277C>T (p.Arg93Cys)	rs370788759	0.00060
NM_006073.4(TRDN):c.1895G>A (p.Arg632Lys)	rs181571822	0.00044
NM_006073.4(TRDN):c.1193A>T (p.Glu398Val)	rs374355537	0.00041
NM_006073.4(TRDN):c.1472-12G>A	rs375364108	0.00036
NM_006073.4(TRDN):c.367G>A (p.Asp123Asn)	rs201021891	0.00036
NM_006073.4(TRDN):c.239C>T (p.Ser80Phe)	rs181287533	0.00015
NM_006073.4(TRDN):c.1627C>A (p.Gln543Lys)	rs9398723	0.00013
NM_006073.4(TRDN):c.1568-4T>A	rs764779610	0.00004
NM_006073.4(TRDN):c.1754G>A (p.Arg585Gln)	rs199986608	0.00003
NM_006073.4(TRDN):c.592A>G (p.Thr198Ala)	rs952211002	0.00003
NM_006073.4(TRDN):c.1220-3C>T	rs773907258	0.00002
NM_006073.4(TRDN):c.1365G>A (p.Glu455=)	rs1452206168

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