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.
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.700 1.000 2 2016 2019
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
Cardiac troponin I measurement
CUI: C0883409
Disease: Cardiac troponin I measurement
14 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 0.700 1.000 1 2019 2019
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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