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: rs17053082
rs17053082
SGCD
1.000 0.080 5 155967220 intron variant C/T snv 5.6E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 1.000 1 2013 2013
dbSNP: rs11960617
rs11960617
SGCD
5 156494033 intron variant C/T snv 1.9E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11960617
rs11960617
SGCD
5 156494033 intron variant C/T snv 1.9E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11960617
rs11960617
SGCD
5 156494033 intron variant C/T snv 1.9E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs32063
rs32063
SGCD
1.000 0.040 5 156638583 intron variant T/C snv 0.25
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2011 2011
dbSNP: rs456290
rs456290
SGCD ; LOC105377673
1.000 0.120 5 156728144 intron variant C/T snv 0.73
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome 		0.700 1.000 1 2011 2011
dbSNP: rs6877490
rs6877490
SGCD
1.000 0.040 5 156638636 intron variant A/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2011 2011