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: rs1322648460
rs1322648460
0.776 0.320 11 35139332 frameshift variant G/- delins
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 1.000 2 2011 2013
dbSNP: rs1322648460
rs1322648460
0.776 0.320 11 35139332 frameshift variant G/- delins
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 1.000 1 2016 2016
dbSNP: rs1322648460
rs1322648460
0.776 0.320 11 35139332 frameshift variant G/- delins
ANOPHTHALMIA AND PULMONARY HYPOPLASIA
0.010 1.000 1 2013 2013
dbSNP: rs1322648460
rs1322648460
0.776 0.320 11 35139332 frameshift variant G/- delins
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
0.010 1.000 1 2011 2011
dbSNP: rs1322648460
rs1322648460
0.776 0.320 11 35139332 frameshift variant G/- delins
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 1.000 1 2016 2016
dbSNP: rs1322648460
rs1322648460
0.776 0.320 11 35139332 frameshift variant G/- delins
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs1322648460
rs1322648460
0.776 0.320 11 35139332 frameshift variant G/- delins
CUI: C0023492
Disease: Leukemia, T-Cell
Leukemia, T-Cell
0.010 1.000 1 2008 2008
dbSNP: rs1322648460
rs1322648460
0.776 0.320 11 35139332 frameshift variant G/- delins
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 1.000 1 2016 2016
dbSNP: rs1322648460
rs1322648460
0.776 0.320 11 35139332 frameshift variant G/- delins
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.010 1.000 1 2016 2016
dbSNP: rs187116
rs187116
1.000 0.080 11 35144253 intron variant G/A snv 0.55
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2013 2013
dbSNP: rs12275533
rs12275533
11 35149480 intron variant G/A snv 2.2E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs353623
rs353623
1.000 0.080 11 35150575 intron variant G/A snv 0.32
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE
0.700 1.000 1 2014 2014
dbSNP: rs353618
rs353618
1.000 0.080 11 35153498 intron variant T/C snv 0.32
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE
0.700 1.000 1 2014 2014
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.040 0.750 4 2016 2019
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.040 0.750 4 2016 2019
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
Malignant neoplasm of colon and/or rectum
0.020 1.000 2 2019 2019
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 1.000 2 2015 2019
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 1.000 2 2019 2019
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
Secondary malignant neoplasm of bone
0.010 1.000 1 2015 2015
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2019 2019
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver
0.010 1.000 1 2019 2019
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs187115
rs187115
0.695 0.320 11 35154612 intron variant T/C snv 0.37
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 1.000 1 2014 2014