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: rs4141463
rs4141463
1.000 0.036 20 14766825 intron variant T/C snp 0.51
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.810 < 0.001 1 2011 2012
dbSNP: rs6110278
rs6110278
20 14407569 intron variant C/T snp 0.26
Platelet mean volume determination (procedure)
0.800 1 2009 2009
dbSNP: rs14135
rs14135
20 14884510 non coding transcript exon variant T/C snp 0.26
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1 2013 2013
dbSNP: rs1475531
rs1475531
20 14886776 intron variant G/T snp 0.62
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1 2013 2013
dbSNP: rs200752
rs200752
20 15618886 intron variant G/A,C snp 0.11; 6.4E-05
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1 2012 2012
dbSNP: rs200759
rs200759
20 15625776 intron variant T/C snp 0.13
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.700 1 2012 2012
dbSNP: rs6079468
rs6079468
1.000 0.036 20 14517750 intron variant A/C,T snp 0.17; 3.2E-05
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
0.700 1 2013 2013
dbSNP: rs6110458
rs6110458
20 14882326 intron variant C/T snp 0.25
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1 2013 2013
dbSNP: rs433078
rs433078
20 15419339 intron variant A/G snp 0.52
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 0