Source: ALL

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: rs1380514442
rs1380514442
14 104780205 missense variant T/C snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 1.000 1 2015 2015
dbSNP: rs2494748
rs2494748
14 104792555 intron variant C/T snv 0.51 0.48
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs2494748
rs2494748
14 104792555 intron variant C/T snv 0.51 0.48
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs2498794
rs2498794
14 104778914 intron variant A/G snv 0.54
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2015 2015
dbSNP: rs2498794
rs2498794
14 104778914 intron variant A/G snv 0.54
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2015 2015
dbSNP: rs61759760
rs61759760
14 104789850 intron variant C/T snv 0.31
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.100 1.000 14 2008 2019
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.770 1.000 7 2008 2019
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.060 1.000 6 2013 2019
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.050 1.000 5 2008 2017
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0023418
Disease: leukemia
leukemia
0.050 1.000 5 2007 2010
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.040 1.000 4 2008 2016
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0085261
Disease: Proteus Syndrome
Proteus Syndrome
0.730 1.000 4 2008 2019
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.030 1.000 3 2008 2015
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
0.030 1.000 3 2007 2008
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.030 1.000 3 2008 2017
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0280100
Disease: Solid Neoplasm
Solid Neoplasm
0.030 1.000 3 2015 2018
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.030 1.000 3 2008 2019
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.020 1.000 2 2009 2010
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0025286
Disease: Meningioma
Meningioma
0.020 0.500 2 2013 2020
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.020 1.000 2 2007 2010
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.010 1.000 1 2011 2011
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
Oestrogen receptor positive breast cancer
0.010 1.000 1 2017 2017
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C3282896
Disease: Glandular papilloma
Glandular papilloma
0.010 1.000 1 2018 2018
dbSNP: rs121434592
rs121434592
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06
CUI: C0007097
Disease: Carcinoma
Carcinoma
0.010 1.000 1 2010 2010