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: rs12027135
rs12027135
MACO1
1 25449242 intron variant A/T snv 0.50
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.800 1.000 2 2010 2019
dbSNP: rs12027135
rs12027135
MACO1
1 25449242 intron variant A/T snv 0.50
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2010 2018
dbSNP: rs10903129
rs10903129
MACO1
1 25442446 intron variant A/G snv 0.58
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2009 2018
dbSNP: rs12027135
rs12027135
MACO1
1 25449242 intron variant A/T snv 0.50
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 2 2010 2013
dbSNP: rs10903129
rs10903129
MACO1
1 25442446 intron variant A/G snv 0.58
CUI: C1619634
Disease: erythrocyte sedimentation rate result
erythrocyte sedimentation rate result 		0.700 1.000 1 2011 2011
dbSNP: rs873308
rs873308
RHCE ; MACO1
1 25432164 intron variant G/A snv 0.44
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2009 2009