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: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2013 2013
dbSNP: rs4908760
rs4908760
RERE
1.000 0.040 1 8466082 intron variant G/A snv 0.68
CUI: C0042900
Disease: Vitiligo
Vitiligo 		0.800 1.000 1 2010 2012
dbSNP: rs159963
rs159963
RERE
1.000 0.040 1 8444361 intron variant C/A snv 0.52
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2016 2019
dbSNP: rs172531
rs172531
RERE
1.000 0.040 1 8435530 intron variant A/G snv 0.31
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
dbSNP: rs301797
rs301797
RERE ; RERE-AS1
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: rs301819
rs301819
RERE
0.882 0.120 1 8441726 intron variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 2 2019 2019
dbSNP: rs11121210
rs11121210
RERE
1 8648470 intron variant T/C snv 0.65
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs11121240
rs11121240
RERE
1.000 0.080 1 8834298 intron variant A/T snv 0.51
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs11581328
rs11581328
RERE
1 8447713 intron variant G/A snv 0.16
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
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: rs142472947
rs142472947
RERE
1 8460428 intron variant AAG/- delins 0.16
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
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: rs159962
rs159962
RERE ; RERE-AS1
1 8430923 intron variant C/T snv 0.30
CUI: C0518026
Disease: body fat percentage (physical finding)
body fat percentage (physical finding) 		0.700 1.000 1 2019 2019
dbSNP: rs159963
rs159963
RERE
1.000 0.040 1 8444361 intron variant C/A snv 0.52
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs159963
rs159963
RERE
1.000 0.040 1 8444361 intron variant C/A snv 0.52
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
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: 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: 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: rs301798
rs301798
RERE ; RERE-AS1
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
RERE ; RERE-AS1
1.000 0.040 1 8428505 non coding transcript exon variant A/G snv 0.30
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs301799
rs301799
RERE ; RERE-AS1
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: rs301803
rs301803
RERE
1 8438620 intron variant A/T snv 0.30
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019