rs4453795, FGF12

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.
Phospholipid measurement
CUI: C0202177
Disease: Phospholipid measurement
306 3 192376186 intron variant A/G;T snv 0.700 1.000 1 2008 2008
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 3 192376186 intron variant A/G;T snv 0.700 1.000 1 2008 2008