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: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0004096
Disease: Asthma
Asthma
0.710 1.000 1 2011 2013
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.040 0.750 4 2013 2017
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.040 0.750 4 2013 2017
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C1960398
Disease: HER2-positive carcinoma of breast
HER2-positive carcinoma of breast
0.020 1.000 2 2013 2016
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2019 2019
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma
0.010 1.000 1 2015 2015
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma
0.010 1.000 1 2015 2015
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial
0.010 1.000 1 2005 2005
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.010 1.000 1 2009 2009
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2008 2008
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 1.000 1 2013 2013
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.010 < 0.001 1 2018 2018
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2008 2008
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2008 2008
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.010 1.000 1 2009 2009
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C4733095
Disease: HER2-negative breast cancer
HER2-negative breast cancer
0.010 1.000 1 2017 2017
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0013595
Disease: Eczema
Eczema
0.010 < 0.001 1 2018 2018
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.010 1.000 1 2016 2016
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C4048328
Disease: cervical cancer
cervical cancer
0.010 1.000 1 2019 2019
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2019 2019
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 1.000 1 2016 2016
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2017 2017
dbSNP: rs1058808
rs1058808
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone
0.010 1.000 1 2015 2015