ClinVar Miner

List of variants in gene GLIS3 reported as uncertain significance for Monogenic diabetes

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_001042413.2(GLIS3):c.232C>G (p.Arg78Gly) rs148168366 0.00178
NM_001042413.2(GLIS3):c.1191G>C (p.Gln397His) rs138497710 0.00163
NM_001042413.2(GLIS3):c.793G>T (p.Val265Phe) rs143192828 0.00087
NM_001042413.2(GLIS3):c.2095C>T (p.Arg699Cys) rs145867412 0.00062
NM_001042413.2(GLIS3):c.2096G>A (p.Arg699His) rs149840771 0.00023
NM_001042413.2(GLIS3):c.1154G>T (p.Gly385Val) rs200959196 0.00019
NM_001042413.2(GLIS3):c.1330C>T (p.Pro444Ser) rs755318788 0.00016
NM_001042413.2(GLIS3):c.275C>T (p.Thr92Ile) rs375931960 0.00015
NM_001042413.2(GLIS3):c.2339G>A (p.Arg780Gln) rs200694226 0.00013
NM_001042413.2(GLIS3):c.106G>A (p.Gly36Arg) rs199788224 0.00012
NM_001042413.2(GLIS3):c.24G>T (p.Met8Ile) rs201804281 0.00009
NM_001042413.2(GLIS3):c.31C>T (p.His11Tyr) rs773069755 0.00004
NM_001042413.2(GLIS3):c.2704C>T (p.Arg902Cys) rs1407324725 0.00002
NM_001042413.2(GLIS3):c.590A>T (p.Asp197Val) rs761151597 0.00001
NM_001042413.2(GLIS3):c.1464C>G (p.Asp488Glu) rs377094207
NM_001042413.2(GLIS3):c.2765A>T (p.Gln922Leu) rs1057524895
NM_001042413.2(GLIS3):c.844C>G (p.Pro282Ala) rs143051164
NM_001042413.2(GLIS3):c.95G>C (p.Arg32Pro) rs375834888

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