ClinVar Miner

List of variants in gene FBXO7 reported as pathogenic for Parkinson disease

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_012179.4(FBXO7):c.1132C>G (p.Arg378Gly) rs71799110
NM_012179.4(FBXO7):c.1144+1G>T rs730880272
NM_012179.4(FBXO7):c.1206_1207dup (p.Arg403fs)
NM_012179.4(FBXO7):c.1492C>T (p.Arg498Ter) rs121918304
NM_012179.4(FBXO7):c.152del (p.Asn51fs) rs1228608709
NM_012179.4(FBXO7):c.65C>T (p.Thr22Met) rs121918305

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