ClinVar Miner

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

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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NM_012179.4(FBXO7):c.-184C>T rs11538371
NM_012179.4(FBXO7):c.1125A>G (p.Leu375=) rs147911892
NM_012179.4(FBXO7):c.1144+9C>T rs199954341
NM_012179.4(FBXO7):c.122+272T>G rs8137714
NM_012179.4(FBXO7):c.1271_1272delinsAT (p.Phe424Tyr) rs1601520476
NM_012179.4(FBXO7):c.1546G>C (p.Asp516His) rs34316445
NM_012179.4(FBXO7):c.345G>A (p.Met115Ile) rs11107
NM_012179.4(FBXO7):c.540A>G (p.Pro180=) rs41311141
NM_012179.4(FBXO7):c.693C>T (p.Ser231=) rs61752254
NM_012179.4(FBXO7):c.949C>T (p.Leu317=) rs9726

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