rs1168013, DOCK7

N. diseases: 6
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 1.000 0.120 1 62531167 intron variant C/G;T snv 0.800 1.000 2 2010 2019
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 1.000 0.120 1 62531167 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 1.000 0.120 1 62531167 intron variant C/G;T snv 0.700 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 1.000 0.120 1 62531167 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 1.000 0.120 1 62531167 intron variant C/G;T snv 0.010 1.000 1 2016 2016
Hypochondroplasia (disorder)
CUI: C0410529
Disease: Hypochondroplasia (disorder)
42 1.000 0.120 1 62531167 intron variant C/G;T snv 0.010 1.000 1 2016 2016