List of variants in gene FKBP10 reported as benign for bone development disease

Minimum submission review status:		Collection method:
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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_021939.4(FKBP10):c.*402T>A	rs1043002	0.75914
NM_021939.4(FKBP10):c.*421C>G	rs1043005	0.75834
NM_021939.4(FKBP10):c.*422C>G	rs1043007	0.75828
NM_021939.4(FKBP10):c.590A>G (p.Lys197Arg)	rs34764749	0.06739
NM_021939.4(FKBP10):c.732A>G (p.Thr244=)	rs8078775	0.01623
NM_021939.4(FKBP10):c.1400-4C>G	rs114199361	0.01571
NM_021939.4(FKBP10):c.917+53G>T	rs141387386	0.00927
NM_021939.4(FKBP10):c.1256+14G>C	rs202121419	0.00906
NM_021939.4(FKBP10):c.1546G>A (p.Glu516Lys)	rs76022961	0.00741
NM_021939.4(FKBP10):c.1374G>A (p.Pro458=)	rs201069033	0.00040
NM_021939.4(FKBP10):c.1014C>T (p.Arg338=)	rs143903650	0.00031
NM_021939.4(FKBP10):c.492G>A (p.Pro164=)	rs529337443	0.00001
NM_021939.4(FKBP10):c.1256+17dup	rs55720039
NM_021939.4(FKBP10):c.21C>T (p.Pro7=)	rs781985978
NM_021939.4(FKBP10):c.363C>T (p.Pro121=)	rs782356839
NM_021939.4(FKBP10):c.906C>A (p.Leu302=)	rs1597907695
NM_021939.4(FKBP10):c.99C>A (p.Arg33=)	rs1597902330

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