rs11893842, OBSL1;INHA

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.
Agenesis of corpus callosum
CUI: C0175754
Disease: Agenesis of corpus callosum
45 0.925 0.160 2 219572251 intron variant A/G snv 0.45 0.010 1.000 1 2014 2014
Aplasia Cutis Congenita
CUI: C0282160
Disease: Aplasia Cutis Congenita
14 0.925 0.160 2 219572251 intron variant A/G snv 0.45 0.010 1.000 1 2014 2014