List of variants in gene TSEN34 reported as likely benign for central nervous system malformation

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_024075.4(TSEN34):c.*1177G>T	rs78711269	0.03779
NM_024075.4(TSEN34):c.*1176A>T	rs78793520	0.02245
NM_024075.5(TSEN34):c.-5+15G>A	rs141003293	0.00497
NM_001077446.4(TSEN34):c.*1053G>A	rs182704571	0.00428
NM_024075.5(TSEN34):c.-95A>G	rs115290127	0.00390
NM_001077446.4(TSEN34):c.314G>A (p.Arg105Gln)	rs138586360	0.00024
NM_001077446.4(TSEN34):c.*385A>T	rs36622

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