rs7134594, MMAB

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 1.000 0.200 12 109562388 intron variant C/G;T snv 0.800 1.000 5 2010 2019
Serum HDL cholesterol measurement
CUI: C0428472
Disease: Serum HDL cholesterol measurement
679 1.000 0.200 12 109562388 intron variant C/G;T snv 0.700 1.000 2 2010 2013
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 1.000 0.200 12 109562388 intron variant C/G;T snv 0.700 1.000 1 2018 2018
Deficiency of mevalonate kinase
CUI: C0342731
Disease: Deficiency of mevalonate kinase
23 1.000 0.200 12 109562388 intron variant C/G;T snv 0.010 1.000 1 2018 2018