List of variants in gene HNF1A reported as likely benign for Monogenic diabetes

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.1165T>G (p.Leu389Val)	rs115080759	0.00198
NM_000545.8(HNF1A):c.1722C>A (p.Ser574Arg)	rs141304623	0.00103
NM_000545.8(HNF1A):c.142G>A (p.Glu48Lys)	rs772222326	0.00009
NM_000545.8(HNF1A):c.871C>T (p.Pro291Ser)	rs151256267	0.00006
NM_000545.8(HNF1A):c.1383C>T (p.Pro461=)	rs772756175	0.00004
NM_000545.8(HNF1A):c.1663C>T (p.Leu555Phe)	rs193922587	0.00001
NM_000545.8(HNF1A):c.766T>A (p.Ser256Thr)	rs781711191	0.00001
NM_000545.8(HNF1A):c.1544C>A (p.Thr515Lys)	rs745460046
NM_000545.8(HNF1A):c.306C>T (p.Ala102=)	rs1486966222
NM_000545.8(HNF1A):c.872C>A (p.Pro291Gln)	rs193922606

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