Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs887569
rs887569
0.882 0.120 7 148808210 intron variant C/T snv 0.73
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.020 1.000 2 2016 2018
dbSNP: rs887569
rs887569
0.882 0.120 7 148808210 intron variant C/T snv 0.73
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.020 1.000 2 2016 2018
dbSNP: rs10274701
rs10274701
0.925 0.080 7 148855364 intron variant C/T snv 0.76
CUI: C3539878
Disease: Triple Negative Breast Neoplasms
Triple Negative Breast Neoplasms
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10274701
rs10274701
0.925 0.080 7 148855364 intron variant C/T snv 0.76
CUI: C4722518
Disease: Triple-Negative Breast Carcinoma
Triple-Negative Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs10952780
rs10952780
7 148857243 intron variant A/C snv 0.46
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs10952780
rs10952780
7 148857243 intron variant A/C snv 0.46
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs12670401
rs12670401
0.925 0.080 7 148865843 intron variant T/C snv 0.41
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs12670401
rs12670401
0.925 0.080 7 148865843 intron variant T/C snv 0.41
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2010 2010
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2010 2010
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2010 2010
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
Secondary malignant neoplasm of colon and/or rectum
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2015 2015
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
Malignant neoplasm of urinary bladder
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2016 2016
dbSNP: rs3757441
rs3757441
0.752 0.200 7 148827660 intron variant C/T snv 0.80
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs6464926
rs6464926
0.882 0.120 7 148821919 intron variant C/T snv 0.41
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs6464926
rs6464926
0.882 0.120 7 148821919 intron variant C/T snv 0.41
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs6464926
rs6464926
0.882 0.120 7 148821919 intron variant C/T snv 0.41
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2018 2018
dbSNP: rs6464926
rs6464926
0.882 0.120 7 148821919 intron variant C/T snv 0.41
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs734004
rs734004
0.925 0.080 7 148808368 intron variant G/C snv 0.66
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014