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: rs1057519913
rs1057519913
0.925 0.120 1 11157172 missense variant G/C snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519913
rs1057519913
0.925 0.120 1 11157172 missense variant G/C snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519914
rs1057519914
0.851 0.240 1 11157174 missense variant A/G snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519914
rs1057519914
0.851 0.240 1 11157174 missense variant A/G snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519914
rs1057519914
0.851 0.240 1 11157174 missense variant A/G snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519915
rs1057519915
0.851 0.160 1 11109318 missense variant A/C snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519915
rs1057519915
0.851 0.160 1 11109318 missense variant A/C snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519915
rs1057519915
0.851 0.160 1 11109318 missense variant A/C snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057519915
rs1057519915
0.851 0.160 1 11109318 missense variant A/C snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519916
rs1057519916
0.882 0.160 1 11109320 missense variant T/A snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057519916
rs1057519916
0.882 0.160 1 11109320 missense variant T/A snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519916
rs1057519916
0.882 0.160 1 11109320 missense variant T/A snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519916
rs1057519916
0.882 0.160 1 11109320 missense variant T/A snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519917
rs1057519917
0.807 0.160 1 11124517 missense variant A/G;T snv
CUI: C0017636
Disease: Glioblastoma
Glioblastoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519917
rs1057519917
0.807 0.160 1 11124517 missense variant A/G;T snv
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs1057519917
rs1057519917
0.807 0.160 1 11124517 missense variant A/G;T snv
Papillary renal cell carcinoma, sporadic
0.700 1.000 1 2016 2016
dbSNP: rs1057519917
rs1057519917
0.807 0.160 1 11124517 missense variant A/G;T snv
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519917
rs1057519917
0.807 0.160 1 11124517 missense variant A/G;T snv
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma
0.700 1.000 1 2016 2016
dbSNP: rs1057519917
rs1057519917
0.807 0.160 1 11124517 missense variant A/G;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs1057519917
rs1057519917
0.807 0.160 1 11124517 missense variant A/G;T snv
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs11581010
rs11581010
1 11152401 non coding transcript exon variant A/G snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs12139042
rs12139042
1 11107089 3 prime UTR variant G/A snv 5.7E-02 5.0E-02
CUI: C0524957
Disease: Corneal Topography
Corneal Topography
0.700 1.000 1 2014 2014
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: rs28991009
rs28991009
1 11193627 missense variant G/A;T snv 1.6E-05; 3.4E-03
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018