rs774005786, PARK7

N. diseases: 8
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 7, AUTOSOMAL RECESSIVE EARLY-ONSET
7 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 0.700 1.000 12 2003 2013
Young onset Parkinson disease
CUI: C4275179
Disease: Young onset Parkinson disease
32 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 0.020 1.000 2 2004 2010
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 0.020 1.000 2 2005 2013
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 0.010 1.000 1 2005 2005
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 0.010 1.000 1 2005 2005
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 0.010 1.000 1 2005 2005
PARKINSON DISEASE, LATE-ONSET
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
76 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 0.010 1.000 1 2005 2005
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.790 0.080 1 7970951 missense variant G/A;T snv 3.9E-04; 2.0E-05 0.010 1.000 1 2008 2008