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.
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
240 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.800 1 2002 2002
melanoma
CUI: C0025202
Disease: melanoma
389 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.720 1.000 9 2002 2016
Follicular thyroid carcinoma
CUI: C0206682
Disease: Follicular thyroid carcinoma
20 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.720 1.000 2 2012 2016
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
35 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.710 1.000 2 2016 2016
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
362 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.700 2 2002 2013
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
428 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.700 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
223 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.700 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
96 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.700 1 2016 2016
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
228 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.700 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
103 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.700 1 2004 2004
Colorectal Cancer
CUI: C1527249
Disease: Colorectal Cancer
955 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.700 1 2002 2002
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
203 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.700 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
149 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.700 1 2016 2016
Cardio-facio-cutaneous syndrome
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
56 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.700 1 2009 2009
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
74 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.060 1.000 6 2004 2016
Thyroid Gland Follicular Adenoma
CUI: C0151468
Disease: Thyroid Gland Follicular Adenoma
4 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.020 1.000 2 2003 2016
Follicular adenoma
CUI: C0205647
Disease: Follicular adenoma
2 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.020 1.000 2 2003 2016
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
129 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.020 0.500 2 2006 2016
Follicular neoplasm
CUI: C0474808
Disease: Follicular neoplasm
3 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.010 1.000 1 2013 2013
Thyroid Nodule
CUI: C0040137
Disease: Thyroid Nodule
8 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.010 1.000 1 2016 2016
Papillary and follicular adenocarcinoma
2 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.010 1.000 1 2017 2017
Papillary carcinoma, clear cell
CUI: C1720430
Disease: Papillary carcinoma, clear cell
2 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.010 1.000 1 2017 2017
Poorly differentiated carcinoma
CUI: C0741899
Disease: Poorly differentiated carcinoma
2 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.010 1.000 1 2017 2017
Splenic Marginal Zone B-Cell Lymphoma
3 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.010 1.000 1 2012 2012
Follicular Variant Thyroid Gland Papillary Carcinoma
2 0.652 0.429 7 140753334 missense variant T/C,G snp 4.0E-06 0.010 1.000 1 2017 2017