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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001048166.1(STIL):c.257C>T (p.Ala86Val)	rs3125630	0.58260
NM_001048166.1(STIL):c.2615+27A>G	rs2742104	0.43900
NM_001048166.1(STIL):c.1024-4T>C	rs188900275	0.00229
NM_001048166.1(STIL):c.1069G>A (p.Ala357Thr)	rs75426387	0.00194
NM_001048166.1(STIL):c.1455G>C (p.Leu485Phe)	rs139912214	0.00193
NM_001048166.1(STIL):c.1005A>G (p.Glu335=)	rs149296029	0.00030
NM_001048166.1(STIL):c.2259C>G (p.Ser753=)	rs774035449	0.00008
NM_001048166.1(STIL):c.3437C>T (p.Ala1146Val)	rs3766317	0.00007
NM_001048166.1(STIL):c.428T>C (p.Val143Ala)	rs200768902	0.00006
NM_001048166.1(STIL):c.2880G>A (p.Pro960=)	rs774354721	0.00001
NM_001048166.1(STIL):c.2383+11dup	rs757631449
NM_001048166.1(STIL):c.3321G>C (p.Gly1107=)	rs1553167547

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