List of variants in gene HNF1B reported as uncertain risk allele for Maturity onset diabetes mellitus in young

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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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000458.4(HNF1B):c.1025C>T (p.Ser342Phe)	rs780035561	0.00001
NM_000458.4(HNF1B):c.1057A>G (p.Ser353Gly)	rs753847783	0.00001
NM_000458.4(HNF1B):c.1117G>A (p.Ala373Thr)	rs759270956	0.00001
NM_000458.4(HNF1B):c.146C>G (p.Ser49Cys)	rs770078634	0.00001
NM_000458.4(HNF1B):c.345-11T>G	rs200782591	0.00001
NM_000458.4(HNF1B):c.1180A>G (p.Asn394Asp)	rs2032897142
NM_000458.4(HNF1B):c.1340-3C>T	rs2032559501
NM_000458.4(HNF1B):c.1663C>A (p.Gln555Lys)	rs886044437
NM_000458.4(HNF1B):c.262A>G (p.Thr88Ala)	rs1555833051
NM_000458.4(HNF1B):c.298A>T (p.Thr100Ser)	rs1568675935
NM_000458.4(HNF1B):c.325G>C (p.Glu109Gln)	rs757044850
NM_000458.4(HNF1B):c.339G>A (p.Met113Ile)	rs764079701
NM_000458.4(HNF1B):c.364G>A (p.Ala122Thr)	rs1568670778
NM_000458.4(HNF1B):c.479T>G (p.Met160Arg)	rs886043903
NM_000458.4(HNF1B):c.61G>A (p.Val21Ile)	rs1304695155
NM_000458.4(HNF1B):c.972C>A (p.His324Gln)	rs753631084
NM_000458.4(HNF1B):c.983C>G (p.Pro328Arg)	rs764132839

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