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: 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: 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: rs17036350
rs17036350
1 11111169 intron variant C/T snv 9.5E-02 9.6E-02
CUI: C0524957
Disease: Corneal Topography
Corneal Topography
0.800 1.000 1 2011 2011
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
dbSNP: rs2300092
rs2300092
1 11206407 intron variant T/C snv 0.55
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2791643
rs2791643
1 11147212 intron variant C/T snv 0.66
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs3806317
rs3806317
0.925 0.080 1 11188159 intron variant A/G snv 3.4E-02
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.010 1.000 1 2013 2013
dbSNP: rs3806317
rs3806317
0.925 0.080 1 11188159 intron variant A/G snv 3.4E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2013 2013
dbSNP: rs74225573
rs74225573
1 11220937 intron variant T/C;G snv
CUI: C0524957
Disease: Corneal Topography
Corneal Topography
0.800 1.000 1 2014 2014
dbSNP: rs1057519914
rs1057519914
0.851 0.240 1 11157174 missense variant A/G snv
CUI: C1846385
Disease: FOCAL CORTICAL DYSPLASIA OF TAYLOR
FOCAL CORTICAL DYSPLASIA OF TAYLOR
0.700 1.000 4 2015 2016