List of variants in gene combination HNF1B, LOC126862549 reported as likely benign for disorder of glycolysis

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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_000458.4(HNF1B):c.809+109A>G	rs9901538	0.01153
NM_000458.4(HNF1B):c.660T>C (p.Asp220=)	rs779375959	0.00008
NM_000458.4(HNF1B):c.723G>A (p.Ala241=)	rs768490293	0.00004
NM_000458.4(HNF1B):c.699C>T (p.Arg233=)	rs1365215108	0.00001
NM_000458.4(HNF1B):c.618T>C (p.Phe206=)
NM_000458.4(HNF1B):c.621A>G (p.Pro207=)
NM_000458.4(HNF1B):c.657C>T (p.Ser219=)	rs148713761
NM_000458.4(HNF1B):c.684C>G (p.Asn228Lys)
NM_000458.4(HNF1B):c.703C>A (p.Arg235=)	rs193922491
NM_000458.4(HNF1B):c.708C>T (p.Phe236=)

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