Source: GWASDB

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: rs6110278
rs6110278
20 14407569 intron variant C/T snv 0.27
Platelet mean volume determination (procedure)
0.800 1.000 1 2009 2009
dbSNP: rs4141463
rs4141463
0.925 0.040 20 14766825 intron variant T/C snv 0.50
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.820 0.667 1 2010 2019
dbSNP: rs200744
rs200744
20 15613722 intron variant C/T snv 0.12
CUI: C0524957
Disease: Corneal Topography
Corneal Topography
0.700 1.000 1 2011 2011
dbSNP: rs200752
rs200752
20 15618886 intron variant G/A;C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2011 2011
dbSNP: rs200759
rs200759
20 15625776 intron variant T/C snv 0.12
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1.000 1 2011 2011
dbSNP: rs14135
rs14135
1.000 0.040 20 14884510 non coding transcript exon variant T/C snv 0.26
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs1475531
rs1475531
1.000 0.040 20 14886776 intron variant G/T snv 0.62
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs6110458
rs6110458
1.000 0.040 20 14882326 intron variant C/T snv 0.25
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs6079468
rs6079468
1.000 0.040 20 14517750 intron variant A/C;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 1.000 1 2013 2013