Source: CURATED

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: rs12331851
rs12331851
1.000 0.040 4 145928143 intron variant G/A snv 7.1E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs12518194
rs12518194
1.000 0.040 5 25951452 intergenic variant A/G snv 0.27
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2009 2009
dbSNP: rs12519594
rs12519594
1.000 0.040 5 25934696 intergenic variant G/A snv 0.27
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2009 2009
dbSNP: rs12521157
rs12521157
1.000 0.040 5 25869292 intergenic variant C/T snv 0.28
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2009 2009
dbSNP: rs12521388
rs12521388
1.000 0.040 5 25912004 downstream gene variant G/A snv 0.29
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2009 2009
dbSNP: rs12701862
rs12701862
1.000 0.040 7 41083854 intergenic variant G/A snv 0.68
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs12726299
rs12726299
1.000 0.040 1 115983051 intron variant G/A snv 0.46
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs13166776
rs13166776
1.000 0.040 5 25971247 intron variant T/C snv 0.28
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2009 2009
dbSNP: rs13176113
rs13176113
1.000 0.040 5 25900331 intergenic variant G/A snv 0.28
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2009 2009
dbSNP: rs13187934
rs13187934
1.000 0.040 5 25902259 intergenic variant C/T snv 0.28
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2009 2009
dbSNP: rs1346536
rs1346536
1.000 0.040 5 25915543 downstream gene variant A/G;T snv
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2009 2009
dbSNP: rs1408744
rs1408744
1.000 0.040 6 23789887 intergenic variant A/G snv 0.63
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
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: rs1429793
rs1429793
1.000 0.040 11 20904710 intron variant G/C;T snv
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2013 2013
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: rs16919315
rs16919315
1.000 0.040 12 125599817 intron variant C/A;G;T snv
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs17007739
rs17007739
1.000 0.040 4 83920097 intron variant T/G snv 0.38
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs17134117
rs17134117
1.000 0.040 7 3991432 intron variant C/T snv 9.1E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2013 2013
dbSNP: rs1718101
rs1718101
1.000 0.040 7 146425696 intron variant T/C;G snv
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs17482975
rs17482975
1.000 0.040 5 25901499 intergenic variant C/T snv 0.28
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2009 2009
dbSNP: rs1877455
rs1877455
1.000 0.040 1 114556471 intergenic variant C/T snv 0.12
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.810 1.000 1 2014 2014
dbSNP: rs1879532
rs1879532
1.000 0.040 2 211574587 intron variant T/A;C;G snv
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs1895729
rs1895729
1.000 0.040 11 107113002 intergenic variant G/A snv 0.37
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs1896731
rs1896731
1.000 0.040 5 25898911 intergenic variant T/C snv 0.38
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2009 2009
dbSNP: rs1930165
rs1930165
1.000 0.040 10 54542170 intron variant G/A;C snv
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012