Source: GWASDB

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: rs12145833
rs12145833
SDCCAG8
1.000 0.080 1 243320452 intron variant T/G snv 0.11
CUI: C0028754
Disease: Obesity
Obesity 		0.800 1.000 1 2010 2010
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 1 2013 2019
dbSNP: rs1538774
rs1538774
SDCCAG8
1.000 0.040 1 243381525 intron variant C/G snv 0.78
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 1 2013 2013
dbSNP: rs6703335
rs6703335
SDCCAG8
0.882 0.040 1 243445665 intron variant A/G snv 0.50
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.800 1.000 1 2011 2013
dbSNP: rs6429427
rs6429427
AKT3 ; SDCCAG8
1 243493899 intron variant T/C snv 3.9E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6429427
rs6429427
AKT3 ; SDCCAG8
1 243493899 intron variant T/C snv 3.9E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6429427
rs6429427
AKT3 ; SDCCAG8
1 243493899 intron variant T/C snv 3.9E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012