rs2854744, IGFBP3

N. diseases: 20
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.040 0.500 4 2007 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.030 1.000 3 2007 2016
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.030 1.000 3 2007 2016
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.020 1.000 2 2011 2012
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.020 1.000 2 2011 2012
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.020 1.000 2 2012 2018
Acromegaly
CUI: C0001206
Disease: Acromegaly
25 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2018 2018
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2011 2011
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2012 2012
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2011 2011
Erectile dysfunction
CUI: C0242350
Disease: Erectile dysfunction
44 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2013 2013
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2015 2015
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2010 2010
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2012 2012
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2015 2015
Polyp of large intestine
CUI: C0949059
Disease: Polyp of large intestine
32 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2010 2010
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2012 2012
Somatotropin deficiency
CUI: C0271561
Disease: Somatotropin deficiency
14 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2009 2009
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2015 2015
Turner Syndrome
CUI: C0041408
Disease: Turner Syndrome
21 0.695 0.520 7 45921476 intron variant G/T snv 0.48 0.010 1.000 1 2012 2012