Source: GWASCAT

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: rs301797
rs301797
1.000 0.040 1 8427263 intron variant C/A snv 0.30
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 2 2015 2019
dbSNP: rs159962
rs159962
1 8430923 intron variant C/T snv 0.30
body fat percentage (physical finding)
0.700 1.000 1 2019 2019
dbSNP: rs301798
rs301798
1.000 0.040 1 8428505 non coding transcript exon variant A/G snv 0.30
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2017 2017
dbSNP: rs301798
rs301798
1.000 0.040 1 8428505 non coding transcript exon variant A/G snv 0.30
Child Development Disorders, Pervasive
0.700 1.000 1 2017 2017
dbSNP: rs301799
rs301799
1.000 0.040 1 8429242 intron variant C/T snv 0.61
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2019 2019
dbSNP: rs301807
rs301807
0.925 0.080 1 8424763 intron variant A/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs301807
rs301807
0.925 0.080 1 8424763 intron variant A/G;T snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs301807
rs301807
0.925 0.080 1 8424763 intron variant A/G;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.700 1.000 1 2016 2016
dbSNP: rs301807
rs301807
0.925 0.080 1 8424763 intron variant A/G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2018 2018
dbSNP: rs302714
rs302714
1 8426071 intron variant A/C snv 0.27
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2019 2019
dbSNP: rs302719
rs302719
1.000 0.040 1 8430260 intron variant T/G snv 0.33
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 1.000 1 2019 2019
dbSNP: rs302719
rs302719
1.000 0.040 1 8430260 intron variant T/G snv 0.33
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 1.000 1 2019 2019