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: rs1034528
rs1034528
0.882 0.120 1 11189075 intron variant G/C snv 0.30
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2016 2016
dbSNP: rs1034528
rs1034528
0.882 0.120 1 11189075 intron variant G/C snv 0.30
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2016 2016
dbSNP: rs1034528
rs1034528
0.882 0.120 1 11189075 intron variant G/C snv 0.30
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs1034528
rs1034528
0.882 0.120 1 11189075 intron variant G/C snv 0.30
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2013 2013
dbSNP: rs1034528
rs1034528
0.882 0.120 1 11189075 intron variant G/C snv 0.30
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.010 1.000 1 2019 2019
dbSNP: rs1064261
rs1064261
0.925 0.080 1 11228701 missense variant G/A;T snv 0.75; 4.0E-06
CUI: C0346429
Disease: Multiple malignancy
Multiple malignancy
0.010 1.000 1 2015 2015
dbSNP: rs1064261
rs1064261
0.925 0.080 1 11228701 missense variant G/A;T snv 0.75; 4.0E-06
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 1.000 1 2015 2015
dbSNP: rs1064261
rs1064261
0.925 0.080 1 11228701 missense variant G/A;T snv 0.75; 4.0E-06
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs11121704
rs11121704
1 11233902 intron variant C/A;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2014 2014
dbSNP: rs11121704
rs11121704
1 11233902 intron variant C/A;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2014 2014
dbSNP: rs11121704
rs11121704
1 11233902 intron variant C/A;T snv
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 1.000 1 2014 2014
dbSNP: rs118203945
rs118203945
0.882 0.280 1 11273836 missense variant A/G snv
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect
0.010 1.000 1 2018 2018
dbSNP: rs118203945
rs118203945
0.882 0.280 1 11273836 missense variant A/G snv
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
0.010 1.000 1 2018 2018
dbSNP: rs12125777
rs12125777
0.925 0.080 1 11261608 intron variant C/T snv 5.1E-02
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2016 2016
dbSNP: rs12125777
rs12125777
0.925 0.080 1 11261608 intron variant C/T snv 5.1E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs17036508
rs17036508
0.925 0.080 1 11195977 3 prime UTR variant T/C snv 9.0E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2016 2016
dbSNP: rs17036508
rs17036508
0.925 0.080 1 11195977 3 prime UTR variant T/C snv 9.0E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2016 2016
dbSNP: rs1883965
rs1883965
0.807 0.160 1 11262099 intron variant A/G snv 0.63
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs1883965
rs1883965
0.807 0.160 1 11262099 intron variant A/G snv 0.63
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.010 1.000 1 2018 2018
dbSNP: rs1883965
rs1883965
0.807 0.160 1 11262099 intron variant A/G snv 0.63
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2016 2016
dbSNP: rs1883965
rs1883965
0.807 0.160 1 11262099 intron variant A/G snv 0.63
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.010 1.000 1 2018 2018
dbSNP: rs1883965
rs1883965
0.807 0.160 1 11262099 intron variant A/G snv 0.63
Malignant neoplasm of urinary bladder
0.010 1.000 1 2018 2018
dbSNP: rs1883965
rs1883965
0.807 0.160 1 11262099 intron variant A/G snv 0.63
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2013 2013
dbSNP: rs1883965
rs1883965
0.807 0.160 1 11262099 intron variant A/G snv 0.63
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2016 2016
dbSNP: rs1883965
rs1883965
0.807 0.160 1 11262099 intron variant A/G snv 0.63
Squamous cell carcinoma of esophagus
0.010 1.000 1 2013 2013