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: rs10205350
rs10205350
1.000 0.040 2 30923631 intron variant G/T snv 0.24
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs10489525
rs10489525
1.000 0.040 1 114721064 intron variant G/A snv 0.32
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.800 1.000 1 2014 2014
dbSNP: rs11102800
rs11102800
1.000 0.040 1 114498310 intron variant C/T snv 0.58
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.800 1.000 1 2014 2014
dbSNP: rs11118968
rs11118968
1.000 0.040 1 206524916 intron variant G/A snv 7.5E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs11211996
rs11211996
1.000 0.040 11 106987949 intron variant T/C snv 0.15
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs11582563
rs11582563
1.000 0.040 1 114416918 intron variant G/A snv 0.14
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.800 1.000 1 2014 2014
dbSNP: rs11585926
rs11585926
1.000 0.040 1 114431068 intron variant T/C snv 0.22
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.800 1.000 1 2014 2014
dbSNP: rs11589568
rs11589568
1.000 0.040 1 114453702 intron variant T/C snv 0.14
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.800 1.000 1 2014 2014
dbSNP: rs12194182
rs12194182
1.000 0.040 6 160413483 intron variant T/C snv 0.21
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
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: 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: 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: 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: 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
dbSNP: rs2056412
rs2056412
1.000 0.040 8 138401090 intron variant T/C snv 0.14
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2013 2013
dbSNP: rs2150291
rs2150291
1.000 0.040 14 63864705 intron variant T/C snv 0.81
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs263025
rs263025
1.000 0.040 3 183809830 intron variant T/C snv 0.45
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs263035
rs263035
1.000 0.040 3 183805869 intron variant A/G snv 0.44
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012
dbSNP: rs2836439
rs2836439
ERG
1.000 0.040 21 38493226 intron variant C/T snv 0.16
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.700 1.000 1 2012 2012