List of variants in gene SZT2 reported as likely benign for not specified

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001365999.1(SZT2):c.2631C>T (p.Thr877=)	rs140831372	0.00717
NM_001365999.1(SZT2):c.6543A>G (p.Leu2181=)	rs112461557	0.00596
NM_001365999.1(SZT2):c.4531G>A (p.Val1511Ile)	rs76675748	0.00361
NM_001365999.1(SZT2):c.7245C>T (p.Ser2415=)	rs142822908	0.00173
NM_001365999.1(SZT2):c.7395T>C (p.Ile2465=)	rs78858677	0.00134
NM_001365999.1(SZT2):c.8427G>A (p.Glu2809=)	rs140309222	0.00088
NM_001365999.1(SZT2):c.2037+14T>C	rs183998762	0.00009
NM_001365999.1(SZT2):c.8817C>T (p.Pro2939=)	rs777808688	0.00006
NM_001365999.1(SZT2):c.9360T>C (p.Ser3120=)	rs367855839	0.00004
NM_001365999.1(SZT2):c.8151+11C>T	rs78750047	0.00001
NM_001365999.1(SZT2):c.1770-11C>T	rs756655876
NM_001365999.1(SZT2):c.6039T>C (p.Tyr2013=)	rs1192938717
NM_001365999.1(SZT2):c.7020G>A (p.Pro2340=)	rs375793150

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