List of variants reported as uncertain significance for Diabetes mellitus type 1; Type 1 diabetes mellitus 20; Maturity-onset diabetes of the young type 3; Type 2 diabetes mellitus; Hepatic adenomas, familial; Nonpapillary renal cell carcinoma

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		ClinVar version:

Total variants: 106

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.1501+6C>T	rs374306837	0.00035
NM_000545.8(HNF1A):c.524A>G (p.Gln175Arg)	rs147400498	0.00018
NM_000545.8(HNF1A):c.1756G>A (p.Ala586Thr)	rs373857078	0.00017
NM_000545.8(HNF1A):c.716C>T (p.Ala239Val)	rs587778397	0.00016
NC_000012.12:g.120978511A>G	rs756136537	0.00015
NM_000545.8(HNF1A):c.1706G>A (p.Ser569Asn)	rs752219487	0.00011
NM_000545.8(HNF1A):c.341G>A (p.Arg114His)	rs139016696	0.00007
NM_000545.8(HNF1A):c.542G>C (p.Gly181Ala)	rs773315874	0.00007
NM_000545.8(HNF1A):c.1405C>T (p.His469Tyr)	rs201811844	0.00006
NM_000545.8(HNF1A):c.1849G>A (p.Val617Ile)	rs146855738	0.00006
NM_000545.8(HNF1A):c.245C>T (p.Thr82Met)	rs568123980	0.00006
NM_000545.8(HNF1A):c.236A>T (p.Glu79Val)	rs143753579	0.00004
NM_000545.8(HNF1A):c.481G>A (p.Ala161Thr)	rs201095611	0.00004
NM_000545.8(HNF1A):c.962G>A (p.Arg321His)	rs751761766	0.00004
NM_000545.8(HNF1A):c.1322C>A (p.Thr441Lys)	rs371544082	0.00003
NM_000545.8(HNF1A):c.139G>C (p.Gly47Arg)	rs373180062	0.00003
NM_000545.8(HNF1A):c.467C>T (p.Thr156Met)	rs150513055	0.00003
NM_000545.8(HNF1A):c.499G>A (p.Val167Ile)	rs371759652	0.00003
NM_000545.8(HNF1A):c.125G>A (p.Gly42Asp)	rs1261968643	0.00002
NM_000545.8(HNF1A):c.1400C>T (p.Pro467Leu)	rs764483607	0.00002
NM_000545.8(HNF1A):c.1504C>G (p.Leu502Val)	rs924150546	0.00002
NM_000545.8(HNF1A):c.1576G>A (p.Asp526Asn)	rs1315721381	0.00002
NM_000545.8(HNF1A):c.1745A>G (p.His582Arg)	rs193922589	0.00002
NM_000545.8(HNF1A):c.1774T>C (p.Ser592Pro)	rs1352126690	0.00002
NM_000545.8(HNF1A):c.29C>T (p.Thr10Met)	rs774637975	0.00002
NM_000545.8(HNF1A):c.923C>T (p.Pro308Leu)	rs754306821	0.00002
NM_000545.8(HNF1A):c.1030G>A (p.Val344Met)	rs767616383	0.00001
NM_000545.8(HNF1A):c.1159C>T (p.His387Tyr)	rs1403526456	0.00001
NM_000545.8(HNF1A):c.140G>A (p.Gly47Glu)	rs1391743259	0.00001
NM_000545.8(HNF1A):c.1513C>A (p.His505Asn)	rs577078110	0.00001
NM_000545.8(HNF1A):c.1537A>T (p.Thr513Ser)	rs753702603	0.00001
NM_000545.8(HNF1A):c.1555C>T (p.Pro519Ser)	rs200639058	0.00001
NM_000545.8(HNF1A):c.1573A>T (p.Thr525Ser)	rs759717253	0.00001
NM_000545.8(HNF1A):c.1637A>C (p.Asp546Ala)	rs984428675	0.00001
NM_000545.8(HNF1A):c.1769T>C (p.Val590Ala)	rs928744634	0.00001
NM_000545.8(HNF1A):c.1778G>C (p.Ser593Thr)	rs200120574	0.00001
NM_000545.8(HNF1A):c.1824C>G (p.Ser608Arg)	rs1877445147	0.00001
NM_000545.8(HNF1A):c.257T>A (p.Leu86His)	rs200442958	0.00001
NM_000545.8(HNF1A):c.340C>T (p.Arg114Cys)	rs774996577	0.00001
NM_000545.8(HNF1A):c.713+14C>T	rs193922601	0.00001
NM_000545.8(HNF1A):c.780G>A (p.Thr260=)	rs749633685	0.00001
NM_000545.8(HNF1A):c.865C>A (p.Pro289Thr)	rs765829022	0.00001
NM_000545.8(HNF1A):c.884C>T (p.Pro295Leu)	rs747958319	0.00001
NM_000545.8(HNF1A):c.901G>A (p.Ala301Thr)	rs555681479	0.00001
NM_000545.8(HNF1A):c.932C>A (p.Ala311Asp)	rs757574765	0.00001
NM_000545.8(HNF1A):c.-119G>A
NM_000545.8(HNF1A):c.-133_-128dup
NM_000545.8(HNF1A):c.-62C>G
NM_000545.8(HNF1A):c.1036_1056dup (p.Ser352_Pro353insThrProLeuHisGlnValSer)
NM_000545.8(HNF1A):c.1107+6T>C
NM_000545.8(HNF1A):c.1107+9C>T
NM_000545.8(HNF1A):c.1107G>C (p.Leu369=)
NM_000545.8(HNF1A):c.1206C>A (p.Asn402Lys)
NM_000545.8(HNF1A):c.1309+16T>C
NM_000545.8(HNF1A):c.1322C>T (p.Thr441Met)
NM_000545.8(HNF1A):c.1361G>A (p.Ser454Asn)
NM_000545.8(HNF1A):c.1424C>T (p.Pro475Leu)	rs193922580
NM_000545.8(HNF1A):c.1469T>C (p.Met490Thr)
NM_000545.8(HNF1A):c.1474A>G (p.Thr492Ala)
NM_000545.8(HNF1A):c.1512C>A (p.Ser504Arg)
NM_000545.8(HNF1A):c.1526T>C (p.Val509Ala)
NM_000545.8(HNF1A):c.1544C>T (p.Thr515Met)	rs745460046
NM_000545.8(HNF1A):c.154G>A (p.Gly52Ser)
NM_000545.8(HNF1A):c.1610C>T (p.Thr537Met)	rs372624970
NM_000545.8(HNF1A):c.1668_1669delinsAT (p.His556_Thr557delinsGlnSer)
NM_000545.8(HNF1A):c.1717G>T (p.Ala573Ser)
NM_000545.8(HNF1A):c.1720_1721delinsGA (p.Ser574Asp)
NM_000545.8(HNF1A):c.1727A>C (p.Gln576Pro)	rs1877318918
NM_000545.8(HNF1A):c.1768+5G>A
NM_000545.8(HNF1A):c.1789C>T (p.Leu597=)
NM_000545.8(HNF1A):c.1810A>G (p.Ser604Gly)
NM_000545.8(HNF1A):c.1812C>G (p.Ser604Arg)
NM_000545.8(HNF1A):c.181C>T (p.Pro61Ser)
NM_000545.8(HNF1A):c.1825C>T (p.His609Tyr)	rs2135854619
NM_000545.8(HNF1A):c.1838C>T (p.Ser613Phe)
NM_000545.8(HNF1A):c.1854C>G (p.Ile618Met)	rs193922591
NM_000545.8(HNF1A):c.1864A>C (p.Ile622Leu)
NM_000545.8(HNF1A):c.1877T>A (p.Met626Lys)
NM_000545.8(HNF1A):c.216C>G (p.Asp72Glu)
NM_000545.8(HNF1A):c.223G>A (p.Asp75Asn)
NM_000545.8(HNF1A):c.238G>T (p.Asp80Tyr)	rs76845985
NM_000545.8(HNF1A):c.272A>G (p.Asn91Ser)
NM_000545.8(HNF1A):c.283G>A (p.Glu95Lys)	rs1555210473
NM_000545.8(HNF1A):c.354G>A (p.Met118Ile)
NM_000545.8(HNF1A):c.41C>T (p.Ala14Val)	rs772214801
NM_000545.8(HNF1A):c.464A>G (p.Lys155Arg)
NM_000545.8(HNF1A):c.542G>A (p.Gly181Glu)
NM_000545.8(HNF1A):c.548G>C (p.Gly183Ala)
NM_000545.8(HNF1A):c.587C>G (p.Thr196Ser)
NM_000545.8(HNF1A):c.691A>T (p.Thr231Ser)
NM_000545.8(HNF1A):c.845C>A (p.Ala282Asp)
NM_000545.8(HNF1A):c.862G>A (p.Gly288Arg)
NM_000545.8(HNF1A):c.863_864inv (p.Gly288Ala)
NM_000545.8(HNF1A):c.865C>T (p.Pro289Ser)	rs765829022
NM_000545.8(HNF1A):c.869C>A (p.Pro290His)	rs778231679
NM_000545.8(HNF1A):c.871C>A (p.Pro291Thr)	rs151256267
NM_000545.8(HNF1A):c.871C>G (p.Pro291Ala)	rs151256267
NM_000545.8(HNF1A):c.872C>T (p.Pro291Leu)	rs193922606
NM_000545.8(HNF1A):c.893C>T (p.Ala298Val)
NM_000545.8(HNF1A):c.929C>T (p.Pro310Leu)
NM_000545.8(HNF1A):c.932C>G (p.Ala311Gly)
NM_000545.8(HNF1A):c.943A>C (p.Ser315Arg)
NM_000545.8(HNF1A):c.950T>C (p.Val317Ala)
NM_000545.8(HNF1A):c.961C>T (p.Arg321Cys)
NM_000545.8(HNF1A):c.973C>A (p.Pro325Thr)
NM_000545.8(HNF1A):c.977C>T (p.Ala326Val)	rs369764257

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