ClinVar Miner

List of variants in gene GLIS3 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001042413.2(GLIS3):c.1270T>C (p.Ser424Pro) rs806052 0.99890
NM_001042413.2(GLIS3):c.1367C>A (p.Pro456Gln) rs6415788 0.62075
NM_001042413.2(GLIS3):c.2686C>T (p.Leu896Phe) rs76094493 0.03919
NM_001042413.2(GLIS3):c.1536C>A (p.Asp512Glu) rs148199056 0.01645
NM_001042413.2(GLIS3):c.938G>C (p.Gly313Ala) rs35154632 0.01104
NM_001042413.2(GLIS3):c.171C>T (p.Asn57=) rs117802495 0.00947
NM_001042413.2(GLIS3):c.1545G>C (p.Glu515Asp) rs72687988 0.00304
NM_001042413.2(GLIS3):c.2089G>A (p.Val697Met) rs148816140 0.00229
NM_001042413.2(GLIS3):c.893C>A (p.Ser298Tyr) rs148572278 0.00199
NM_001042413.2(GLIS3):c.1092G>T (p.Pro364=) rs74680081 0.00172
NM_001042413.2(GLIS3):c.954C>T (p.Thr318=) rs75564360 0.00165
NM_001042413.2(GLIS3):c.1044C>T (p.Tyr348=) rs146238548 0.00086
NM_001042413.2(GLIS3):c.2340G>A (p.Arg780=) rs147473975 0.00086
NM_001042413.2(GLIS3):c.61A>G (p.Arg21Gly) rs199527360 0.00086
NM_001042413.2(GLIS3):c.1872C>T (p.Thr624=) rs140309338 0.00068
NM_001042413.2(GLIS3):c.2096G>A (p.Arg699His) rs149840771 0.00023
NM_001042413.2(GLIS3):c.1395T>C (p.His465=) rs752606768 0.00006
NM_001042413.2(GLIS3):c.2159G>A (p.Arg720Gln) rs200316055 0.00005
NM_001042413.2(GLIS3):c.1263C>T (p.Asp421=) rs755713904 0.00003
GRCh37/hg19 9p24.2(chr9:3543768-4334707)
GRCh37/hg19 9p24.2(chr9:3691055-3837855)
GRCh37/hg19 9p24.2(chr9:3898270-4246395)x1
NM_001042413.2(GLIS3):c.1471G>A (p.Gly491Arg) rs562740663
NM_001042413.2(GLIS3):c.3G>A (p.Met1Ile) rs1198183960

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.