DOCK7, dedicator of cytokinesis 7, 85440

N. diseases: 51; N. variants: 192
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2131925
rs2131925
1 62560271 intron variant G/T snv 0.57
Low density lipoprotein cholesterol measurement
0.800 1.000 5 2010 2019
dbSNP: rs2131925
rs2131925
1 62560271 intron variant G/T snv 0.57
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 5 2010 2019
dbSNP: rs10889353
rs10889353
1 62652525 intron variant A/C;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2009 2019
dbSNP: rs11207995
rs11207995
1 62583880 intron variant A/C;G snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2013 2019
dbSNP: rs1748195
rs1748195
0.851 0.120 1 62583922 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 4 2008 2019
dbSNP: rs2131925
rs2131925
1 62560271 intron variant G/T snv 0.57
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2010 2019
dbSNP: rs10889353
rs10889353
1 62652525 intron variant A/C;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2009 2019
dbSNP: rs1167998
rs1167998
1 62465961 intron variant C/A snv 0.57
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 3 2009 2019
dbSNP: rs1748195
rs1748195
0.851 0.120 1 62583922 intron variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 3 2012 2019
dbSNP: rs1167998
rs1167998
1 62465961 intron variant C/A snv 0.57
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2012 2019
dbSNP: rs1167998
rs1167998
1 62465961 intron variant C/A snv 0.57
Low density lipoprotein cholesterol measurement
0.800 1.000 2 2012 2019
dbSNP: rs1168013
rs1168013
1.000 0.120 1 62531167 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 1.000 2 2010 2019
dbSNP: rs1168029
rs1168029
1 62503731 intron variant G/A;C snv
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
0.800 1.000 1 2012 2012
dbSNP: rs10889348
rs10889348
1 62612551 intron variant A/T snv 0.32
Low density lipoprotein cholesterol measurement
0.700 1.000 3 2015 2019
dbSNP: rs9988450
rs9988450
1 62458777 non coding transcript exon variant C/T snv 0.39
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 3 2015 2019
dbSNP: rs10889348
rs10889348
1 62612551 intron variant A/T snv 0.32
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2019
dbSNP: rs10889348
rs10889348
1 62612551 intron variant A/T snv 0.32
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs11207995
rs11207995
1 62583880 intron variant A/C;G snv
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs11207995
rs11207995
1 62583880 intron variant A/C;G snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2018 2019
dbSNP: rs12042319
rs12042319
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 2 2016 2019
dbSNP: rs12042319
rs12042319
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2016 2019
dbSNP: rs1479675678
rs1479675678
1.000 1 62513588 stop gained G/A;C snv 7.0E-06
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2006 2014
dbSNP: rs1553163123
rs1553163123
1.000 1 62528151 splice region variant C/T snv
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
0.700 1.000 2 2006 2014
dbSNP: rs1748195
rs1748195
0.851 0.120 1 62583922 intron variant C/G;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 2 2018 2019
dbSNP: rs1748197
rs1748197
1 62590441 intron variant G/A snv 0.42
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 2 2012 2012