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: 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: rs115683961
rs115683961
ERBB4
2 211521195 intron variant A/G snv 3.9E-02
CUI: C0523677
Disease: Glycine measurement
Glycine measurement 		0.700 1.000 1 2019 2019
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: rs13428799
rs13428799
ERBB4
2 212537150 intron variant C/G snv 1.7E-02
CUI: C0428419
Disease: Triiodothyronine measurement
Triiodothyronine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs1394780
rs1394780
ERBB4
2 212418466 intron variant T/G snv 0.24
CUI: C0202231
Disease: Thyroxine measurement
Thyroxine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs16825008
rs16825008
ERBB4
2 211440116 intron variant A/G snv 0.27
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1949651
rs1949651
ERBB4
2 212252904 intron variant C/T snv 0.43
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs2220024
rs2220024
ERBB4
2 212467655 intron variant A/G snv 0.43
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs3791699
rs3791699
ERBB4
2 211409722 intron variant G/A snv 0.27
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs4132462
rs4132462
ERBB4
2 211770864 intron variant C/T snv 0.24
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
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: 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