rs13079920, RBMS3

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.
Chromosome 11p11.2 Deletion Syndrome
CUI: C1832588
Disease: Chromosome 11p11.2 Deletion Syndrome
6 0.882 0.200 3 29404440 intron variant G/A;T snv 0.010 1.000 1 2016 2016
PEELING SKIN SYNDROME
CUI: C1849193
Disease: PEELING SKIN SYNDROME
11 0.882 0.200 3 29404440 intron variant G/A;T snv 0.010 1.000 1 2016 2016
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.882 0.200 3 29404440 intron variant G/A;T snv 0.010 1.000 1 2016 2016