List of variants in gene FKBP10 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_021939.4(FKBP10):c.1667G>A (p.Arg556His)	rs138281924	0.00120
NM_021939.4(FKBP10):c.1256C>T (p.Ser419Leu)	rs146422412	0.00107
NM_021939.4(FKBP10):c.850G>A (p.Gly284Arg)	rs372214186	0.00023
NM_021939.4(FKBP10):c.473T>C (p.Val158Ala)	rs781874365	0.00009
NM_021939.4(FKBP10):c.1556C>T (p.Pro519Leu)	rs140883152	0.00007
NM_021939.4(FKBP10):c.587G>A (p.Ser196Asn)	rs782660556	0.00002
NM_021939.4(FKBP10):c.1160G>A (p.Arg387Gln)	rs782107514	0.00001
NM_021939.4(FKBP10):c.1640T>C (p.Ile547Thr)	rs368139860	0.00001
NM_021939.4(FKBP10):c.311G>A (p.Arg104Gln)	rs142507953	0.00001
NM_021939.4(FKBP10):c.505C>T (p.Arg169Cys)	rs782676847	0.00001
NM_021939.4(FKBP10):c.781G>A (p.Val261Met)	rs781821453	0.00001
NM_021939.4(FKBP10):c.1207C>G (p.Arg403Gly)	rs372896892
NM_021939.4(FKBP10):c.1373C>T (p.Pro458Leu)
NM_021939.4(FKBP10):c.1582G>T (p.Ala528Ser)	rs1255679632
NM_021939.4(FKBP10):c.829C>G (p.Pro277Ala)	rs138089753

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