rs3862434, CRTC3

N. diseases: 3
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 1.000 0.080 15 90537155 intron variant A/G snv 0.48 0.010 1.000 1 2014 2014
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 1.000 0.080 15 90537155 intron variant A/G snv 0.48 0.010 1.000 1 2014 2014
SVEINSSON CHORIORETINAL ATROPHY
CUI: C1862382
Disease: SVEINSSON CHORIORETINAL ATROPHY
30 1.000 0.080 15 90537155 intron variant A/G snv 0.48 0.010 1.000 1 2018 2018