List of variants in gene HNF1A reported as likely pathogenic by Genetics and Molecular Pathology, SA Pathology

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.404del (p.Asp135fs)	rs2135832632
NM_000545.8(HNF1A):c.475C>T (p.Arg159Trp)	rs765432081
NM_000545.8(HNF1A):c.661C>T (p.Gln221Ter)	rs2135839643

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