List of variants in gene HNF1B reported as uncertain significance by Personalized Diabetes Medicine Program, University of Maryland School of Medicine

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000458.4(HNF1B):c.1373T>G (p.Val458Gly)	rs375644184	0.00002
NM_000458.4(HNF1B):c.1630A>G (p.Thr544Ala)	rs1352906725	0.00001
NM_000458.4(HNF1B):c.1180A>G (p.Asn394Asp)	rs2032897142
NM_000458.4(HNF1B):c.244G>A (p.Asp82Asn)
NM_000458.4(HNF1B):c.262A>G (p.Thr88Ala)	rs1555833051
NM_000458.4(HNF1B):c.499G>C (p.Ala167Pro)	rs757452269

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