List of variants in gene GLIS3 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_001042413.2(GLIS3):c.1318A>G (p.Thr440Ala)	rs80161424	0.00314
NM_001042413.2(GLIS3):c.1545G>C (p.Glu515Asp)	rs72687988	0.00304
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.1090C>T (p.Pro364Ser)	rs143056249	0.00165
NM_001042413.2(GLIS3):c.954C>T (p.Thr318=)	rs75564360	0.00165
NM_001042413.2(GLIS3):c.1509C>T (p.Arg503=)	rs141125402	0.00103
NM_001042413.2(GLIS3):c.1044C>T (p.Tyr348=)	rs146238548	0.00086
NM_001042413.2(GLIS3):c.1872C>T (p.Thr624=)	rs140309338	0.00068
NM_001042413.2(GLIS3):c.1452G>A (p.Gln484=)	rs143229804	0.00060
NM_001042413.2(GLIS3):c.1056G>C (p.Leu352=)	rs140880100	0.00029
NM_001042413.2(GLIS3):c.105C>T (p.Ser35=)	rs372340726	0.00009
NM_001042413.2(GLIS3):c.645G>A (p.Thr215=)	rs142323958	0.00008
NM_001042413.2(GLIS3):c.1368A>T (p.Pro456=)	rs755087869	0.00005
NM_001042413.2(GLIS3):c.1272G>A (p.Ser424=)	rs764287243	0.00001
NM_001042413.2(GLIS3):c.273C>T (p.Leu91=)
NM_001042413.2(GLIS3):c.630G>A (p.Thr210=)

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