List of variants in gene HNF1A reported as likely benign for not specified

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: 47

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.51C>G (p.Leu17=)	rs1169289	0.42543
NM_000545.8(HNF1A):c.79A>C (p.Ile27Leu)	rs1169288	0.35489
NM_000545.8(HNF1A):c.1501+7G>A	rs2464195	0.30441
NM_000545.8(HNF1A):c.1460G>A (p.Ser487Asn)	rs2464196	0.26206
NM_000545.8(HNF1A):c.1375C>T (p.Leu459=)	rs2259820	0.26141
NM_000545.8(HNF1A):c.1545G>A (p.Thr515=)	rs55834942	0.13864
NM_000545.5(HNF1A):c.-347G>A	rs76729898	0.00231
NM_000545.8(HNF1A):c.1165T>G (p.Leu389Val)	rs115080759	0.00198
NM_000545.8(HNF1A):c.1446C>T (p.Ser482=)	rs147366495	0.00117
NM_000545.6(HNF1A):c.-527C>T	rs3809315	0.00115
NM_000545.8(HNF1A):c.-29G>A	rs376961226	0.00108
NM_000545.8(HNF1A):c.1323G>A (p.Thr441=)	rs138996307	0.00081
NM_000545.8(HNF1A):c.1748G>A (p.Arg583Gln)	rs137853242	0.00060
NM_000545.8(HNF1A):c.965A>G (p.Tyr322Cys)	rs140491072	0.00041
NM_000545.8(HNF1A):c.1539C>T (p.Thr513=)	rs193922584	0.00037
NM_000545.8(HNF1A):c.336G>A (p.Pro112=)	rs371365341	0.00036
NM_000545.8(HNF1A):c.1386C>T (p.Val462=)	rs143015301	0.00021
NM_000545.8(HNF1A):c.1377G>A (p.Leu459=)	rs118028009	0.00020
NM_000545.8(HNF1A):c.1500C>T (p.His500=)	rs201694197	0.00017
NM_000545.8(HNF1A):c.693G>A (p.Thr231=)	rs145240086	0.00017
NM_000545.8(HNF1A):c.521C>T (p.Ala174Val)	rs201934320	0.00013
NM_000545.8(HNF1A):c.1624-19G>A	rs193922586	0.00011
NM_000545.8(HNF1A):c.1593C>T (p.Ser531=)	rs370300688	0.00008
NM_000545.8(HNF1A):c.1729C>G (p.His577Asp)	rs376832928	0.00006
NM_000545.8(HNF1A):c.1015G>A (p.Gly339Ser)	rs766790596	0.00004
NM_000545.8(HNF1A):c.1383C>T (p.Pro461=)	rs772756175	0.00004
NM_000545.8(HNF1A):c.1502-14T>C	rs765596650	0.00004
NM_000545.8(HNF1A):c.1624-15G>A	rs193922585	0.00004
NM_000545.8(HNF1A):c.1522G>A (p.Glu508Lys)	rs483353044	0.00003
NM_000545.8(HNF1A):c.900C>T (p.Pro300=)	rs762555237	0.00003
NM_000545.8(HNF1A):c.1745A>G (p.His582Arg)	rs193922589	0.00002
NM_000545.8(HNF1A):c.216C>T (p.Asp72=)	rs148961412	0.00002
NM_000545.8(HNF1A):c.1623+20G>A	rs1012229716	0.00001
NM_000545.8(HNF1A):c.246G>A (p.Thr82=)	rs752243228	0.00001
NM_000545.8(HNF1A):c.685C>A (p.Arg229=)	rs769086289	0.00001
NM_000545.8(HNF1A):c.1107+6T>C
NM_000545.8(HNF1A):c.1135C>G (p.Pro379Ala)	rs754729248
NM_000545.8(HNF1A):c.1309+16T>C
NM_000545.8(HNF1A):c.1341G>A (p.Pro447=)
NM_000545.8(HNF1A):c.1548C>T (p.Gly516=)	rs886038346
NM_000545.8(HNF1A):c.1623+16G>A	rs1555212572
NM_000545.8(HNF1A):c.1623+3A>G	rs886038347
NM_000545.8(HNF1A):c.1689C>G (p.Thr563=)
NM_000545.8(HNF1A):c.1761C>T (p.Ser587=)	rs2135851686
NM_000545.8(HNF1A):c.306C>T (p.Ala102=)	rs1486966222
NM_000545.8(HNF1A):c.840G>A (p.Lys280=)	rs1876974758
NM_000545.8(HNF1A):c.872C>A (p.Pro291Gln)	rs193922606

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