rs1009977, LGALS3

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.
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 1.000 0.040 14 55136284 intron variant T/G snv 0.48 0.700 1.000 1 2012 2012
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 1.000 0.040 14 55136284 intron variant T/G snv 0.48 0.010 1.000 1 2018 2018