rs755588390, PRKN

N. diseases: 7
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Bell Palsy
CUI: C0376175
Disease: Bell Palsy
3 0.851 0.160 6 162262672 missense variant T/C;G snv 0.010 1.000 1 2007 2007
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
79 0.851 0.160 6 162262672 missense variant T/C;G snv 0.010 1 2007 2007
Facial paralysis
CUI: C0015469
Disease: Facial paralysis
3 0.851 0.160 6 162262672 missense variant T/C;G snv 0.010 1.000 1 2007 2007
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.851 0.160 6 162262672 missense variant T/C;G snv 0.010 1 2019 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.851 0.160 6 162262672 missense variant T/C;G snv 0.010 1 2019 2019
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.851 0.160 6 162262672 missense variant T/C;G snv 0.010 1 2019 2019
Young onset Parkinson disease
CUI: C4275179
Disease: Young onset Parkinson disease
32 0.851 0.160 6 162262672 missense variant T/C;G snv 0.010 1 2007 2007