Variants in gene HNF1A with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 26

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.1545G>A (p.Thr515=)	rs55834942	0.13864
NM_000545.8(HNF1A):c.92G>A (p.Gly31Asp)	rs137853247	0.00076
NM_000545.8(HNF1A):c.-89T>C	rs767550584	0.00074
NM_000545.8(HNF1A):c.1748G>A (p.Arg583Gln)	rs137853242	0.00060
NM_000545.8(HNF1A):c.1539C>T (p.Thr513=)	rs193922584	0.00037
NM_000545.8(HNF1A):c.1501+6C>T	rs374306837	0.00035
NM_000545.8(HNF1A):c.1309+102A>T	rs113111047	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
NM_000545.8(HNF1A):c.-96T>G	rs576862555	0.00013
NM_000545.8(HNF1A):c.521C>T (p.Ala174Val)	rs201934320	0.00013
NM_000545.8(HNF1A):c.142G>A (p.Glu48Lys)	rs772222326	0.00009
NM_000545.8(HNF1A):c.-181G>A	rs980850048	0.00007
NM_000545.8(HNF1A):c.1502-14T>C	rs765596650	0.00004
NM_000545.8(HNF1A):c.527-18G>A	rs375259151	0.00004
NM_000545.8(HNF1A):c.1745A>G (p.His582Arg)	rs193922589	0.00002
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.-124G>C	rs563304627
NM_000545.8(HNF1A):c.-167TGGGGGT[3]	rs538476099
NM_000545.8(HNF1A):c.1135C>G (p.Pro379Ala)	rs754729248
NM_000545.8(HNF1A):c.1380_1406del (p.Gln460_Leu468del)	rs544842497
NM_000545.8(HNF1A):c.1424C>T (p.Pro475Leu)	rs193922580
NM_000545.8(HNF1A):c.1502-19CT[2]	rs753496283
NM_000545.8(HNF1A):c.155_156delinsCT (p.Gly52Ala)	rs587778393
NM_000545.8(HNF1A):c.872C>A (p.Pro291Gln)	rs193922606

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