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: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0850639
Disease: premalignant lesion
premalignant lesion
0.010 < 0.001 1 2005 2005
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
0.010 < 0.001 1 2018 2018
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0085695
Disease: Chronic gastritis
Chronic gastritis
0.010 < 0.001 1 2005 2005
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid
0.020 0.500 2 2009 2015
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.020 0.500 2 2009 2018
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm
0.020 0.500 2 2009 2015
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0025202
Disease: melanoma
melanoma
0.020 0.500 2 2010 2016
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.020 0.500 2 2009 2015
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.020 0.500 2 2014 2014
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.100 0.636 22 2004 2019
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.100 0.636 22 2004 2019
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.100 0.636 22 2004 2019
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.030 0.667 3 2010 2016
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.030 0.667 3 2014 2016
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
0.030 0.667 3 2014 2016
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.080 0.750 8 2004 2015
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.080 0.750 8 2004 2015
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone
0.040 0.750 4 2015 2018
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma
0.040 0.750 4 2015 2018
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.040 0.750 4 2011 2014
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma
0.040 0.750 4 2015 2018
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.100 0.846 13 2004 2019
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 0.846 13 2004 2019
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
Xeroderma Pigmentosum, Complementation Group D
0.070 0.857 7 2003 2014
dbSNP: rs861539
rs861539
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.070 0.857 7 2011 2015