List of variants in gene HNF1B reported as uncertain significance for not specified

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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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000458.4(HNF1B):c.1654-9T>A	rs200579660	0.00009
NM_000458.4(HNF1B):c.1339+17G>A	rs374854968	0.00006
NM_000458.4(HNF1B):c.313G>A (p.Glu105Lys)	rs199572129	0.00006
NM_000458.3(HNF1B):c.-338C>A	rs935794447	0.00004
NM_000458.4(HNF1B):c.1390G>A (p.Gly464Ser)	rs982085453	0.00002
NM_000458.4(HNF1B):c.1025C>T (p.Ser342Phe)	rs780035561	0.00001
NM_000458.4(HNF1B):c.*111G>C
NM_000458.4(HNF1B):c.-134G>A	rs577836898
NM_000458.4(HNF1B):c.1207-7C>T	rs1215174368
NM_000458.4(HNF1B):c.1339+12T>C	rs1375568430
NM_000458.4(HNF1B):c.140C>T (p.Pro47Leu)
NM_000458.4(HNF1B):c.1441C>G (p.Pro481Ala)	rs2147446997
NM_000458.4(HNF1B):c.1484T>A (p.Met495Lys)
NM_000458.4(HNF1B):c.1508C>T (p.Ala503Val)	rs748568345
NM_000458.4(HNF1B):c.1654-11_1654-9delinsC	rs386134268
NM_000458.4(HNF1B):c.244G>A (p.Asp82Asn)
NM_000458.4(HNF1B):c.254A>G (p.Asp85Gly)	rs984116301
NM_000458.4(HNF1B):c.352C>G (p.Pro118Ala)
NM_000458.4(HNF1B):c.58G>A (p.Gly20Arg)	rs1052557621

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