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: 2

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HGVS	dbSNP
NM_000545.6(HNF1A):c.1748G>A (p.Arg583Gln)	rs137853242
NM_000545.6(HNF1A):c.92G>A (p.Gly31Asp)	rs137853247

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