ClinVar Miner

List of variants in gene FBXO7 reported as benign 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_001033024.1(FBXO7):c.35T>G (p.Leu12Arg) rs8137714
NM_012179.3(FBXO7):c.1144+9C>T rs199954341
NM_012179.3(FBXO7):c.345G>A (p.Met115Ile) rs11107
NM_012179.3(FBXO7):c.540A>G (p.Pro180=) rs41311141
NM_012179.3(FBXO7):c.693C>T (p.Ser231=) rs61752254
NM_012179.3(FBXO7):c.949C>T (p.Leu317=) rs9726

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