rs34424986, PRKN

N. diseases: 10
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.
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
37 0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 0.800 1.000 33 1998 2015
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 0.720 0.500 2 2015 2020
Young onset Parkinson disease
CUI: C4275179
Disease: Young onset Parkinson disease
32 0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 0.710 1.000 19 1999 2016
PARKINSON DISEASE, LATE-ONSET
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
76 0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 0.700 1.000 4 2003 2018
LEPROSY, SUSCEPTIBILITY TO, 2
CUI: C1843632
Disease: LEPROSY, SUSCEPTIBILITY TO, 2
1 0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 0.700 0
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 0.700 0
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 0.020 0.500 2 2015 2020
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 0.020 1.000 2 2005 2018
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 0.020 0.500 2 2015 2020
Mitochondrial abnormalities
CUI: C4020732
Disease: Mitochondrial abnormalities
20 0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 0.010 1.000 1 2007 2007