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: rs16887244
rs16887244
LSM1
1.000 0.040 8 38173827 intron variant A/G snv 0.20
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.810 1.000 1 2011 2011
dbSNP: rs7000184
rs7000184
BAG4 ; LSM1
8 38176676 5 prime UTR variant C/T snv 2.3E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7000184
rs7000184
BAG4 ; LSM1
8 38176676 5 prime UTR variant C/T snv 2.3E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7000184
rs7000184
BAG4 ; LSM1
8 38176676 5 prime UTR variant C/T snv 2.3E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7000184
rs7000184
BAG4 ; LSM1
8 38176676 5 prime UTR variant C/T snv 2.3E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7000184
rs7000184
BAG4 ; LSM1
8 38176676 5 prime UTR variant C/T snv 2.3E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012