rs174537, TMEM258;MYRF

N. diseases: 23
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 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.800 1.000 4 2014 2019
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.800 1.000 2 2008 2018
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 4 2014 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 4 2014 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 4 2014 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 4 2014 2019
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 4 2014 2019
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 4 2014 2019
Malignant neoplasm of large intestine
375 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 4 2014 2019
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 4 2014 2019
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 2 2012 2013
Chronic Kidney Diseases
CUI: C1561643
Disease: Chronic Kidney Diseases
306 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 1 2018 2018
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 1 2015 2015
Fasting blood glucose measurement
CUI: C0428568
Disease: Fasting blood glucose measurement
212 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 1 2012 2012
Fasting blood sugar result
CUI: C1261430
Disease: Fasting blood sugar result
113 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 1 2012 2012
High density lipoprotein measurement
1440 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 1 2018 2018
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.700 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.030 1.000 3 2011 2016
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.010 1 2019 2019
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.010 1.000 1 2016 2016
Familial lichen amyloidosis
CUI: C0268398
Disease: Familial lichen amyloidosis
24 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.010 1.000 1 2016 2016
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.010 1.000 1 2011 2011
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 0.010 1.000 1 2018 2018