rs538622, ERGIC1

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.
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.925 0.120 5 172920676 intron variant A/G snv 0.40 0.010 1.000 1 2018 2018
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.925 0.120 5 172920676 intron variant A/G snv 0.40 0.010 1.000 1 2018 2018