List of variants in gene GLIS3 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001042413.2(GLIS3):c.1318A>G (p.Thr440Ala)	rs80161424	0.00314
NM_001042413.2(GLIS3):c.2340G>A (p.Arg780=)	rs147473975	0.00086
NM_001042413.2(GLIS3):c.744A>G (p.Leu248=)	rs139080385	0.00086
NM_001042413.2(GLIS3):c.1260C>T (p.Pro420=)	rs377419083	0.00059
NM_001042413.2(GLIS3):c.2421C>G (p.Ser807=)	rs563920093	0.00026
NM_001042413.2(GLIS3):c.1327C>T (p.Leu443=)	rs529418802	0.00022
NM_001042413.2(GLIS3):c.1326C>T (p.Asp442=)	rs758928731	0.00010
NM_001042413.2(GLIS3):c.1984-16C>T	rs145670205	0.00008
NM_001042413.2(GLIS3):c.1686T>G (p.Ser562=)	rs745836279	0.00007
NM_001042413.2(GLIS3):c.1395T>C (p.His465=)	rs752606768	0.00006
NM_001042413.2(GLIS3):c.2297+16T>C	rs377104078	0.00005
NM_001042413.2(GLIS3):c.1263C>T (p.Asp421=)	rs755713904	0.00003
NM_001042413.2(GLIS3):c.1272G>A (p.Ser424=)	rs764287243	0.00001
NM_001042413.2(GLIS3):c.555A>C (p.Ala185=)	rs752433935	0.00001
NM_001042413.2(GLIS3):c.2473+13C>T	rs368773221
NM_001042413.2(GLIS3):c.2657-17C>T	rs746005781

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.