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: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.030 1.000 3 2015 2016
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.020 1.000 2 2009 2014
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 1.000 2 2014 2016
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 0.500 2 2015 2018
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.020 1.000 2 2014 2016
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
Squamous cell carcinoma of oropharynx
0.020 1.000 2 2015 2016
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 1.000 2 2013 2019
dbSNP: rs113129609
rs113129609
0.925 0.080 2 112778091 missense variant A/G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 1.000 1 2015 2015
dbSNP: rs113129609
rs113129609
0.925 0.080 2 112778091 missense variant A/G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 < 0.001 1 2003 2003
dbSNP: rs1516792
rs1516792
0.925 0.080 2 112778356 intron variant G/A snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.010 1.000 1 2003 2003
dbSNP: rs1516792
rs1516792
0.925 0.080 2 112778356 intron variant G/A snv
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5
0.010 1.000 1 2003 2003
dbSNP: rs3783525
rs3783525
1.000 0.040 2 112784242 intron variant T/A;C snv
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.010 1.000 1 2015 2015
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0019163
Disease: Hepatitis B
Hepatitis B
0.010 < 0.001 1 2014 2014
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0677886
Disease: Epithelial ovarian cancer
Epithelial ovarian cancer
0.010 1.000 1 2014 2014
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 1.000 1 2016 2016
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2018 2018
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.010 1.000 1 2013 2013
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.010 1.000 1 2016 2016
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.010 1.000 1 2015 2015
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014
dbSNP: rs3783553
rs3783553
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins
CUI: C0279671
Disease: Cervical Squamous Cell Carcinoma
Cervical Squamous Cell Carcinoma
0.010 1.000 1 2015 2015