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: rs12373751
rs12373751
ERBB4
1.000 0.040 2 212072166 intron variant T/C snv 0.62
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.700 1.000 1 2019 2019
dbSNP: rs13019783
rs13019783
ERBB4
1.000 0.040 2 211673690 intron variant T/G snv 9.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1351592
rs1351592
ERBB4
1.000 0.120 2 212529988 intron variant C/G snv 0.29
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.710 1.000 1 2015 2017
dbSNP: rs2178575
rs2178575
ERBB4
1.000 0.120 2 212527042 intron variant G/A;T snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.700 1.000 1 2018 2018
dbSNP: rs35544454
rs35544454
ERBB4
1.000 0.080 2 212401279 intron variant A/T snv 0.14
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2018 2018
dbSNP: rs4423543
rs4423543
ERBB4
1.000 0.040 2 211671321 intron variant G/A snv 0.27
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
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: 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: 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