rs10178332, ROCK2

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.
Respiratory Distress Syndrome, Newborn
37 0.925 0.120 2 11268891 intron variant C/A;G snv 0.010 1.000 1 2017 2017
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.925 0.120 2 11268891 intron variant C/A;G snv 0.010 1.000 1 2016 2016