Variants in gene TRIOBP with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001039141.3(TRIOBP):c.2149C>G (p.Gln717Glu)	rs186620158	0.00221
NM_001039141.3(TRIOBP):c.634G>A (p.Gly212Ser)	rs201794404	0.00115
NM_001039141.3(TRIOBP):c.2811C>T (p.Ile937=)	rs115800799	0.00111
NM_001039141.3(TRIOBP):c.1690A>G (p.Thr564Ala)	rs777175618	0.00097
NM_001039141.3(TRIOBP):c.2201C>T (p.Ser734Phe)	rs199794705	0.00069
NM_001039141.3(TRIOBP):c.1591G>A (p.Ala531Thr)	rs201112075
NM_001039141.3(TRIOBP):c.4703C>G (p.Ala1568Gly)	rs569914227
NM_001039141.3(TRIOBP):c.6472+14G>T	rs45503898

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