Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4764695
rs4764695
HELLPAR ; LINC02456
0.925 0.080 12 102363335 non coding transcript exon variant A/G;T snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.020 1.000 2 2010 2014
dbSNP: rs4764695
rs4764695
HELLPAR ; LINC02456
0.925 0.080 12 102363335 non coding transcript exon variant A/G;T snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.020 1.000 2 2010 2014
dbSNP: rs749124997
rs749124997
IGF1 ; HELLPAR ; LINC02456
1.000 0.040 12 102402539 missense variant C/T snv 4.0E-06
CUI: C0017638
Disease: Glioma
Glioma 		0.010 1.000 1 1999 1999
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone 		0.010 1.000 1 2017 2017
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		0.010 1.000 1 2017 2017
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2015 2015
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0007785
Disease: Cerebral Infarction
Cerebral Infarction 		0.010 1.000 1 2012 2012
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.010 1.000 1 2017 2017
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma 		0.010 1.000 1 2017 2017
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2014 2014
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.010 1.000 1 2017 2017
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma 		0.010 1.000 1 2017 2017
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 1.000 1 2010 2010
dbSNP: rs6218
rs6218
IGF1 ; HELLPAR ; LINC02456
0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		0.010 1.000 1 2015 2015
dbSNP: rs5742714
rs5742714
IGF1 ; HELLPAR ; LINC02456
0.882 0.160 12 102396074 3 prime UTR variant C/G snv 8.9E-02
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs5742714
rs5742714
IGF1 ; HELLPAR ; LINC02456
0.882 0.160 12 102396074 3 prime UTR variant C/G snv 8.9E-02
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.010 1.000 1 2016 2016
dbSNP: rs5742714
rs5742714
IGF1 ; HELLPAR ; LINC02456
0.882 0.160 12 102396074 3 prime UTR variant C/G snv 8.9E-02
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 1.000 1 2010 2010
dbSNP: rs6219
rs6219
IGF1 ; HELLPAR ; LINC02456
1.000 0.080 12 102396414 3 prime UTR variant C/T snv 8.9E-02
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2018 2018
dbSNP: rs6219
rs6219
IGF1 ; HELLPAR ; LINC02456
1.000 0.080 12 102396414 3 prime UTR variant C/T snv 8.9E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2018 2018
dbSNP: rs12426318
rs12426318
HELLPAR
1.000 0.040 12 102241743 non coding transcript exon variant C/A snv 0.18
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.010 1.000 1 2011 2011
dbSNP: rs10860860
rs10860860
HELLPAR ; LINC02456
0.925 0.040 12 102387055 non coding transcript exon variant A/T snv 0.28
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.010 1.000 1 2011 2011
dbSNP: rs10860860
rs10860860
HELLPAR ; LINC02456
0.925 0.040 12 102387055 non coding transcript exon variant A/T snv 0.28
CUI: C0027092
Disease: Myopia
Myopia 		0.010 1.000 1 2011 2011
dbSNP: rs6214
rs6214
IGF1 ; HELLPAR ; LINC02456
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.040 0.500 4 2011 2017