List of variants in gene GTSF1L reported as uncertain significance

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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_176791.4(GTSF1L):c.392C>T (p.Thr131Met)	rs755065790	0.00003
NM_176791.4(GTSF1L):c.440G>C (p.Gly147Ala)	rs749661277	0.00003
NM_176791.4(GTSF1L):c.317T>C (p.Val106Ala)	rs761113372	0.00002
NM_176791.4(GTSF1L):c.189T>G (p.Cys63Trp)	rs760733486	0.00001
NM_176791.4(GTSF1L):c.304G>A (p.Asp102Asn)	rs762812139	0.00001
NM_176791.4(GTSF1L):c.73C>G (p.His25Asp)	rs753261887	0.00001
NM_176791.4(GTSF1L):c.83C>T (p.Ser28Leu)	rs755785059	0.00001
NM_176791.4(GTSF1L):c.128G>A (p.Cys43Tyr)
NM_176791.4(GTSF1L):c.152T>C (p.Val51Ala)	rs1441745572
NM_176791.4(GTSF1L):c.235A>G (p.Lys79Glu)	rs754528433
NM_176791.4(GTSF1L):c.250A>G (p.Ser84Gly)	rs746246690
NM_176791.4(GTSF1L):c.417T>G (p.Ser139Arg)
NM_176791.4(GTSF1L):c.436C>T (p.Pro146Ser)

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