rs9949617, TMEM241

N. diseases: 2
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.
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
169 18 23299253 intron variant C/T snv 0.22 0.700 1.000 1 2013 2013
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 18 23299253 intron variant C/T snv 0.22 0.700 1.000 1 2013 2013