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: rs2252865
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs2252865
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2013 2013
dbSNP: rs2252865
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2013 2013
dbSNP: rs2252865
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2013 2013
dbSNP: rs2252865
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs2252865
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.700 1.000 1 2013 2013
dbSNP: rs34269918
rs34269918
RERE
1.000 0.040 1 8364925 intron variant A/- delins 0.69
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2018 2018
dbSNP: rs3795310
rs3795310
RERE
1.000 0.040 1 8371547 intron variant C/T snv 0.54
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs3795310
rs3795310
RERE
1.000 0.040 1 8371547 intron variant C/T snv 0.54
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs138050288
rs138050288
RERE
1.000 0.120 1 8400188 intron variant CA/- del 0.22
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder) 		0.700 1.000 1 2018 2018
dbSNP: rs55823627
rs55823627
RERE
1 8402019 intron variant C/T snv 0.14
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs301795
rs301795
RERE
1.000 0.040 1 8407293 intron variant G/A snv 0.27
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs159960
rs159960
RERE
1 8416368 intron variant A/G snv 0.45
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs301805
rs301805
RERE
1.000 0.080 1 8420956 intron variant T/G snv 0.65
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs301805
rs301805
RERE
1.000 0.080 1 8420956 intron variant T/G snv 0.65
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2018 2018
dbSNP: rs301805
rs301805
RERE
1.000 0.080 1 8420956 intron variant T/G snv 0.65
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2018 2018
dbSNP: rs301806
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2016 2016
dbSNP: rs301806
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2017 2017
dbSNP: rs301806
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs301806
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62
CUI: C0013595
Disease: Eczema
Eczema 		0.700 1.000 1 2019 2019
dbSNP: rs301807
rs301807
RERE ; RERE-AS1
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
RERE ; RERE-AS1
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
RERE ; RERE-AS1
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
RERE ; RERE-AS1
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
RERE ; RERE-AS1
1 8426071 intron variant A/C snv 0.27
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019