rs12696304, None

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.
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 0.700 1.000 2 2015 2018
Malignant melanoma of skin of lower limb
42 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 0.700 1.000 2 2015 2018
Malignant melanoma of skin of upper limb
42 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 0.700 1.000 2 2015 2018
Lung Diseases, Interstitial
CUI: C0206062
Disease: Lung Diseases, Interstitial
144 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 0.700 1.000 1 2013 2013
Systolic Pressure
CUI: C0871470
Disease: Systolic Pressure
1931 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 0.700 1.000 1 2019 2019
Tooth Attrition
CUI: C0004277
Disease: Tooth Attrition
5 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 0.020 1.000 2 2011 2018
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 0.010 1 2016 2016
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 0.010 1.000 1 2017 2017
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 0.010 1.000 1 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 0.010 1.000 1 2015 2015