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: rs4673628
rs4673628
ERBB4
1.000 0.040 2 211679199 intron variant A/G snv 0.39 0.45
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs4673659
rs4673659
ERBB4
1.000 0.080 2 212325005 intron variant A/C snv 0.69
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2014 2014
dbSNP: rs55897719
rs55897719
ERBB4
2 211726116 intron variant C/A;G snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs62183028
rs62183028
ERBB4
2 211766758 intron variant G/T snv 0.26
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs62183029
rs62183029
ERBB4
2 211767727 intron variant G/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs62183032
rs62183032
ERBB4
1.000 0.040 2 211774137 intron variant A/G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs62183032
rs62183032
ERBB4
1.000 0.040 2 211774137 intron variant A/G;T snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs6435622
rs6435622
ERBB4
2 211431369 intron variant G/C snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs6735626
rs6735626
ERBB4
2 212539248 upstream gene variant G/A;C snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
dbSNP: rs6759039
rs6759039
ERBB4
1.000 0.040 2 211675480 intron variant T/A snv 0.58
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs72948529
rs72948529
ERBB4 ; MTND2P23
1.000 0.040 2 211777265 non coding transcript exon variant A/C snv 0.14
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs74338595
rs74338595
ERBB4
1.000 0.040 2 211885061 intron variant T/C snv 0.23
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs74338595
rs74338595
ERBB4
1.000 0.040 2 211885061 intron variant T/C snv 0.23
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs7583068
rs7583068
ERBB4
1.000 0.040 2 211769383 intron variant T/A snv 0.33
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs7583068
rs7583068
ERBB4
1.000 0.040 2 211769383 intron variant T/A snv 0.33
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs9288447
rs9288447
ERBB4
2 212218913 intron variant T/C snv 0.45
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019