Variants in gene HNF1A with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.1592G>C (p.Ser531Thr)	rs137853246	0.00002
NM_000545.8(HNF1A):c.1501G>A (p.Ala501Thr)	rs371807951	0.00001
NM_000545.8(HNF1A):c.626C>A (p.Ala209Glu)	rs1286294151	0.00001
NM_000545.8(HNF1A):c.1135C>A (p.Pro379Thr)	rs754729248
NM_000545.8(HNF1A):c.1135C>G (p.Pro379Ala)	rs754729248
NM_000545.8(HNF1A):c.608G>T (p.Arg203Leu)	rs587780357
NM_000545.8(HNF1A):c.722G>A (p.Cys241Tyr)	rs2135841113
NM_000545.8(HNF1A):c.827C>A (p.Ala276Asp)	rs137853245

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