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.
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.100 0.882 17 1998 2020
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.070 0.857 7 1998 2020
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
42 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2020 2020
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
56 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.800 0.973 260 1997 2019
HEMOCHROMATOSIS, TYPE 1
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
62 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.900 0.976 248 1996 2019
Hemochromatosis
CUI: C0018995
Disease: Hemochromatosis
45 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.100 0.974 230 1997 2019
Iron Overload
CUI: C0282193
Disease: Iron Overload
53 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.100 0.946 167 1997 2019
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.100 0.895 19 1998 2019
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.100 0.800 15 2000 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.100 0.800 15 2000 2019
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.080 0.875 8 2002 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.080 0.875 8 2003 2019
Cooley's anemia
CUI: C0002875
Disease: Cooley's anemia
19 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.050 1.000 5 2000 2019
Meconium ileus
CUI: C2939175
Disease: Meconium ileus
16 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 1.000 3 1998 2019
Restless Legs Syndrome
CUI: C0035258
Disease: Restless Legs Syndrome
72 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.030 0.667 3 2013 2019
Fatigue
CUI: C0015672
Disease: Fatigue
67 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.020 1.000 2 2008 2019
Back Pain
CUI: C0004604
Disease: Back Pain
10 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2019 2019
Chronic pain
CUI: C0150055
Disease: Chronic pain
19 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2019 2019
Distal ileal obstruction syndrome
CUI: C0854076
Disease: Distal ileal obstruction syndrome
2 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2019 2019
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2019 2019
Malnutrition
CUI: C0162429
Disease: Malnutrition
29 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2019 2019
Polymyalgia Rheumatica
CUI: C0032533
Disease: Polymyalgia Rheumatica
7 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2019 2019
Sarcopenia
CUI: C0872084
Disease: Sarcopenia
10 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.010 1.000 1 2019 2019
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.100 0.970 33 2000 2018
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.100 0.963 27 2000 2018