rs1800435, ALAD

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.
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 0.010 1.000 1 2003 2003
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 0.010 1.000 1 2011 2011
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 0.010 1.000 1 2011 2011
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
79 0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 0.010 1 2017 2017
Neoplasms, Intracranial
CUI: C1527390
Disease: Neoplasms, Intracranial
4 0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 0.010 1.000 1 2005 2005
opioid use
CUI: C0240602
Disease: opioid use
5 0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 0.010 1.000 1 2018 2018
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 0.010 1.000 1 2011 2011