rs3131917, None

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.
Pyloric Stenosis, Hypertrophic
CUI: C0700639
Disease: Pyloric Stenosis, Hypertrophic
306 0.882 0.080 5 173230018 upstream gene variant T/G snv 0.52 0.700 1.000 1 2012 2012
Scleroderma
CUI: C0011644
Disease: Scleroderma
5 0.882 0.080 5 173230018 upstream gene variant T/G snv 0.52 0.010 1.000 1 2018 2018
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.882 0.080 5 173230018 upstream gene variant T/G snv 0.52 0.010 1.000 1 2018 2018