Source: CURATED

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: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2019
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.700 1.000 2 2012 2013
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
0.700 1.000 1 2012 2012
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.700 1.000 1 2018 2018
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
0.700 1.000 1 2018 2018
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
QT interval feature (observable entity)
0.700 1.000 1 2014 2014
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.700 1.000 1 2011 2011
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs174583
rs174583
0.807 0.320 11 61842278 intron variant C/T snv 0.35
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
0.700 1.000 1 2012 2012