List of variants in gene HNRNPK reported as uncertain significance for bone development disease

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_031263.4(HNRNPK):c.1183C>T (p.Pro395Ser)	rs771289643
NM_031263.4(HNRNPK):c.1191+3A>T
NM_031263.4(HNRNPK):c.1198G>A (p.Gly400Arg)
NM_031263.4(HNRNPK):c.1225C>T (p.Arg409Trp)	rs750307456
NM_031263.4(HNRNPK):c.1359C>G (p.Asn453Lys)	rs2133014344
NM_031263.4(HNRNPK):c.1361+7T>G
NM_031263.4(HNRNPK):c.203T>C (p.Leu68Pro)	rs1588432187
NM_031263.4(HNRNPK):c.214-6A>G
NM_031263.4(HNRNPK):c.253G>A (p.Glu85Lys)	rs1554700678
NM_031263.4(HNRNPK):c.455A>T (p.His152Leu)
NM_031263.4(HNRNPK):c.560A>G (p.His187Arg)	rs1588420417
NM_031263.4(HNRNPK):c.709G>A (p.Gly237Ser)
NM_031263.4(HNRNPK):c.779G>A (p.Gly260Asp)	rs757092061

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