rs4665972, SNX17

N. diseases: 9
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.
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 2 27375230 intron variant T/C snv 0.69 0.800 1.000 3 2013 2019
Breast size
CUI: C0425782
Disease: Breast size
38 2 27375230 intron variant T/C snv 0.69 0.800 1.000 1 2012 2012
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 2 27375230 intron variant T/C snv 0.69 0.700 1.000 2 2019 2019
Albuminuria
CUI: C0001925
Disease: Albuminuria
59 2 27375230 intron variant T/C snv 0.69 0.700 1.000 1 2018 2018
Alcohol consumption
CUI: C0001948
Disease: Alcohol consumption
535 2 27375230 intron variant T/C snv 0.69 0.700 1.000 1 2019 2019
Microalbuminuria
CUI: C0730345
Disease: Microalbuminuria
32 2 27375230 intron variant T/C snv 0.69 0.700 1.000 1 2019 2019
Reticulocyte count (procedure)
CUI: C0206161
Disease: Reticulocyte count (procedure)
474 2 27375230 intron variant T/C snv 0.69 0.700 1.000 1 2016 2016
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 2 27375230 intron variant T/C snv 0.69 0.700 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 2 27375230 intron variant T/C snv 0.69 0.700 1.000 1 2019 2019