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: rs3830675
rs3830675
1.000 0.040 10 87931195 intron variant -/TCTTA delins
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.030 1.000 3 2014 2016
dbSNP: rs3830675
rs3830675
1.000 0.040 10 87931195 intron variant -/TCTTA delins
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.030 1.000 3 2014 2016
dbSNP: rs10490920
rs10490920
1.000 0.080 10 87925886 intron variant T/C snv 0.14
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs12242772
rs12242772
10 87944637 intron variant A/G snv 3.0E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12242772
rs12242772
10 87944637 intron variant A/G snv 3.0E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs12242772
rs12242772
10 87944637 intron variant A/G snv 3.0E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs1234214
rs1234214
10 87938433 intron variant C/A snv 0.34
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1234220
rs1234220
0.851 0.080 10 87885716 intron variant A/G snv 9.1E-02
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver
0.010 1.000 1 2015 2015
dbSNP: rs1234220
rs1234220
0.851 0.080 10 87885716 intron variant A/G snv 9.1E-02
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs1234220
rs1234220
0.851 0.080 10 87885716 intron variant A/G snv 9.1E-02
Liver and Intrahepatic Biliary Tract Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs1234220
rs1234220
0.851 0.080 10 87885716 intron variant A/G snv 9.1E-02
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs1234224
rs1234224
0.925 0.040 10 87915539 intron variant A/G snv 0.38
CUI: C0238067
Disease: Colitis, Collagenous
Colitis, Collagenous
0.010 1.000 1 2018 2018
dbSNP: rs1234224
rs1234224
0.925 0.040 10 87915539 intron variant A/G snv 0.38
CUI: C0400821
Disease: Colitis, Microscopic
Colitis, Microscopic
0.010 1.000 1 2018 2018
dbSNP: rs2299939
rs2299939
0.827 0.080 10 87897393 intron variant C/A;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs2299939
rs2299939
0.827 0.080 10 87897393 intron variant C/A;T snv
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs2299939
rs2299939
0.827 0.080 10 87897393 intron variant C/A;T snv
Liver and Intrahepatic Biliary Tract Carcinoma
0.010 < 0.001 1 2015 2015
dbSNP: rs2299939
rs2299939
0.827 0.080 10 87897393 intron variant C/A;T snv
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.010 < 0.001 1 2015 2015
dbSNP: rs2299939
rs2299939
0.827 0.080 10 87897393 intron variant C/A;T snv
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver
0.010 < 0.001 1 2015 2015
dbSNP: rs2299941
rs2299941
0.882 0.080 10 87944962 intron variant A/G snv 9.7E-02
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.010 1.000 1 2018 2018
dbSNP: rs2299941
rs2299941
0.882 0.080 10 87944962 intron variant A/G snv 9.7E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2018 2018
dbSNP: rs2299941
rs2299941
0.882 0.080 10 87944962 intron variant A/G snv 9.7E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs3830675
rs3830675
1.000 0.040 10 87931195 intron variant -/TCTTA delins
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.010 1.000 1 2019 2019
dbSNP: rs3831732
rs3831732
10 87895485 intron variant -/A;AA delins
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs3831732
rs3831732
10 87895485 intron variant -/A;AA delins
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs59085061
rs59085061
10 87921701 intron variant A/G snv 5.2E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019