rs7080536, HABP2;NRAP

N. diseases: 27
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.
THYROID CANCER, NONMEDULLARY, 5
CUI: C4225292
Disease: THYROID CANCER, NONMEDULLARY, 5
1 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.700 0
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2006 2006
Carotid Stenosis
CUI: C0007282
Disease: Carotid Stenosis
19 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2006 2006
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2006 2006
Atherothrombosis
CUI: C1963943
Disease: Atherothrombosis
15 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2008 2008
Deep Vein Thrombosis
CUI: C0149871
Disease: Deep Vein Thrombosis
93 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2008 2008
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
110 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2009 2009
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2009 2009
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2009 2009
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2009 2009
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2009 2009
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
64 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.030 1.000 3 2009 2016
Thyroid Diseases
CUI: C0040128
Disease: Thyroid Diseases
26 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2016 2016
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.040 1.000 4 2016 2017
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.040 1.000 4 2016 2017
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.040 1.000 4 2016 2017
familial non-medullary thyroid cancer
CUI: C4733333
Disease: familial non-medullary thyroid cancer
1 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.020 0.500 2 2017 2017
Familial Nonmedullary Thyroid Cancer
CUI: C3501844
Disease: Familial Nonmedullary Thyroid Cancer
2 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.020 1.000 2 2016 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.020 1.000 2 2016 2017
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2017 2017
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2017 2017
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.010 1.000 1 2017 2017
Familial Nonmedullary Thyroid Gland Carcinoma
CUI: C3896673
Disease: Familial Nonmedullary Thyroid Gland Carcinoma
6 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.040 1.000 4 2016 2018
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.040 1.000 4 2016 2018
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.700 1.000 1 2018 2018