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: rs14403
rs14403
AKT3 ; SDCCAG8
1.000 0.040 1 243500591 3 prime UTR variant C/T snv 0.17
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 3 2013 2019
dbSNP: rs320320
rs320320
AKT3
1 243671884 intron variant A/G snv 0.30
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.800 1.000 1 2013 2013
dbSNP: rs35978510
rs35978510
AKT3
1.000 0.040 1 243612815 non coding transcript exon variant T/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
dbSNP: rs1074657
rs1074657
AKT3
1 243583332 intron variant T/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs12076373
rs12076373
AKT3
1.000 0.040 1 243688645 intron variant G/C snv 0.20
CUI: C0085136
Disease: Central Nervous System Neoplasms
Central Nervous System Neoplasms 		0.700 1.000 1 2017 2017
dbSNP: rs12076373
rs12076373
AKT3
1.000 0.040 1 243688645 intron variant G/C snv 0.20
CUI: C0017638
Disease: Glioma
Glioma 		0.700 1.000 1 2017 2017
dbSNP: rs12093576
rs12093576
AKT3 ; SDCCAG8
1 243492595 intron variant C/T snv 0.47
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs13376709
rs13376709
AKT3
1.000 0.040 1 243527189 intron variant T/C snv 0.52
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2015 2015
dbSNP: rs1973284
rs1973284
AKT3
1 243693379 intron variant A/G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019
dbSNP: rs34770086
rs34770086
AKT3 ; SDCCAG8
1 243503393 3 prime UTR variant CT/- delins 0.29
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs4658403
rs4658403
AKT3
1 243669258 intron variant C/T snv 0.74
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs67027895
rs67027895
AKT3 ; SDCCAG8
1 243503914 3 prime UTR variant C/G;T snv 0.20
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs884328
rs884328
AKT3 ; SDCCAG8
1 243490976 intron variant A/G snv 0.18
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs946824
rs946824
AKT3
1 243520717 intron variant T/C snv 0.87
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019